NO843148L - Fremgangsmaate for fremstilling av dihydrokarbylkarbonater, deres anvendelse som drivstoff-tilsetninger og drivstoffsammensetninger inneholdende disse - Google Patents

Fremgangsmaate for fremstilling av dihydrokarbylkarbonater, deres anvendelse som drivstoff-tilsetninger og drivstoffsammensetninger inneholdende disse

Info

Publication number: NO843148L
Authority: NO; Norway
Prior art keywords: mixture; copper; methanol; carbon monoxide; butanol
Prior art date: 1982-12-15

Application number

NO843148A

Other languages

English (en)

Norwegian (no)

Inventor

George Ernest Morris

Original Assignee

British Petroleum Co Plc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1982-12-15

Filing date

1984-08-06

Publication date

1984-08-06

1983-09-09 Priority claimed from GB838324216A external-priority patent/GB8324216D0/en

1984-08-06 Application filed by British Petroleum Co Plc filed Critical British Petroleum Co Plc

1984-08-06 Publication of NO843148L publication Critical patent/NO843148L/no

Links

239000000203 mixture Substances 0.000 title claims description 62
238000000034 method Methods 0.000 title claims description 21
239000000446 fuel Substances 0.000 title claims description 15
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 title claims description 11
239000002816 fuel additive Substances 0.000 title description 4
238000002360 preparation method Methods 0.000 title description 2
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 78
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 34
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 29
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 28
229910002091 carbon monoxide Inorganic materials 0.000 claims description 28
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 24
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical group CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 claims description 24
239000012969 di-tertiary-butyl peroxide Substances 0.000 claims description 24
239000003054 catalyst Substances 0.000 claims description 17
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 14
239000000654 additive Substances 0.000 claims description 13
150000002978 peroxides Chemical class 0.000 claims description 13
230000000996 additive effect Effects 0.000 claims description 12
IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims description 12
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 11
-1 copper (I) compound Chemical class 0.000 claims description 11
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 10
150000001875 compounds Chemical group 0.000 claims description 10
239000010949 copper Substances 0.000 claims description 10
229910052802 copper Inorganic materials 0.000 claims description 10
238000004519 manufacturing process Methods 0.000 claims description 10
150000004649 carbonic acid derivatives Chemical class 0.000 claims description 7
238000002485 combustion reaction Methods 0.000 claims description 6
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
239000004215 Carbon black (E152) Substances 0.000 claims description 5
125000003118 aryl group Chemical group 0.000 claims description 5
150000004820 halides Chemical class 0.000 claims description 5
229930195733 hydrocarbon Natural products 0.000 claims description 5
150000002430 hydrocarbons Chemical class 0.000 claims description 5
229910017464 nitrogen compound Inorganic materials 0.000 claims description 5
125000002877 alkyl aryl group Chemical group 0.000 claims description 4
125000003710 aryl alkyl group Chemical group 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
150000003333 secondary alcohols Chemical class 0.000 claims description 4
125000000623 heterocyclic group Chemical group 0.000 claims description 3
125000001183 hydrocarbyl group Chemical group 0.000 claims description 3
239000007791 liquid phase Substances 0.000 claims description 3
125000000075 primary alcohol group Chemical group 0.000 claims description 3
239000005749 Copper compound Substances 0.000 claims description 2
150000001880 copper compounds Chemical class 0.000 claims description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 21
238000006243 chemical reaction Methods 0.000 description 20
239000007789 gas Substances 0.000 description 16
OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 9
238000003756 stirring Methods 0.000 description 9
238000001816 cooling Methods 0.000 description 8
ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 8
239000000047 product Substances 0.000 description 8
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 7
KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
229960003280 cupric chloride Drugs 0.000 description 4
239000003085 diluting agent Substances 0.000 description 4
NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
229910021591 Copper(I) chloride Inorganic materials 0.000 description 3
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 3
CNQHQDFYLOARSA-UHFFFAOYSA-N copper;methyl hypochlorite;pyridine Chemical compound [Cu].COCl.C1=CC=NC=C1 CNQHQDFYLOARSA-UHFFFAOYSA-N 0.000 description 3
229910001882 dioxygen Inorganic materials 0.000 description 3
239000002360 explosive Substances 0.000 description 3
238000004817 gas chromatography Methods 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
NTSLROIKFLNUIJ-UHFFFAOYSA-N 5-Ethyl-2-methylpyridine Chemical compound CCC1=CC=C(C)N=C1 NTSLROIKFLNUIJ-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 2
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
238000004821 distillation Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
239000012535 impurity Substances 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
239000001282 iso-butane Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
150000003891 oxalate salts Chemical class 0.000 description 2
239000000575 pesticide Substances 0.000 description 2
239000000376 reactant Substances 0.000 description 2
238000000926 separation method Methods 0.000 description 2
239000002904 solvent Substances 0.000 description 2
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
229910021589 Copper(I) bromide Inorganic materials 0.000 description 1
VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical class [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 description 1
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
QGMRQYFBGABWDR-UHFFFAOYSA-M Pentobarbital sodium Chemical compound [Na+].CCCC(C)C1(CC)C(=O)NC(=O)[N-]C1=O QGMRQYFBGABWDR-UHFFFAOYSA-M 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
PVZPBLDKFOMMNW-UHFFFAOYSA-M [Cl-].N1=CC=CC=C1.CO[Cu+] Chemical compound [Cl-].N1=CC=CC=C1.CO[Cu+] PVZPBLDKFOMMNW-UHFFFAOYSA-M 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
150000004703 alkoxides Chemical class 0.000 description 1
125000005910 alkyl carbonate group Chemical group 0.000 description 1
239000006079 antiknock agent Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
230000033228 biological regulation Effects 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000012459 cleaning agent Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
150000004699 copper complex Chemical class 0.000 description 1
NKNDPYCGAZPOFS-UHFFFAOYSA-M copper(i) bromide Chemical compound Br[Cu] NKNDPYCGAZPOFS-UHFFFAOYSA-M 0.000 description 1
229940045803 cuprous chloride Drugs 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
239000012024 dehydrating agents‎ Substances 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
JMPVESVJOFYWTB-UHFFFAOYSA-N dipropan-2-yl carbonate Chemical compound CC(C)OC(=O)OC(C)C JMPVESVJOFYWTB-UHFFFAOYSA-N 0.000 description 1
JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 description 1
229920006258 high performance thermoplastic Polymers 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000000178 monomer Substances 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
238000005832 oxidative carbonylation reaction Methods 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
150000003057 platinum Chemical class 0.000 description 1
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920003225 polyurethane elastomer Polymers 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000013589 supplement Substances 0.000 description 1
150000008027 tertiary esters Chemical class 0.000 description 1
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
238000010998 test method Methods 0.000 description 1
230000007704 transition Effects 0.000 description 1
229910052723 transition metal Inorganic materials 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Oil, Petroleum & Natural Gas (AREA)
Health & Medical Sciences (AREA)
Emergency Medicine (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Catalysts (AREA)
Liquid Carbonaceous Fuels (AREA)
Solid Fuels And Fuel-Associated Substances (AREA)

NO843148A 1982-12-15 1984-08-06 Fremgangsmaate for fremstilling av dihydrokarbylkarbonater, deres anvendelse som drivstoff-tilsetninger og drivstoffsammensetninger inneholdende disse NO843148L (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB8235694		1982-12-15
GB838324216A GB8324216D0 (en)	1983-09-09	1983-09-09	Additive composition

Publications (1)

Publication Number	Publication Date
NO843148L true NO843148L (no)	1984-08-06

Family

ID=26284692

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO843148A NO843148L (no)	1982-12-15	1984-08-06	Fremgangsmaate for fremstilling av dihydrokarbylkarbonater, deres anvendelse som drivstoff-tilsetninger og drivstoffsammensetninger inneholdende disse

Country Status (10)

Country	Link
EP (1)	EP0112172B1 (fi)
JP (1)	JPS60500259A (fi)
AU (1)	AU570941B2 (fi)
CA (1)	CA1218670A (fi)
DE (1)	DE3372858D1 (fi)
FI (1)	FI843139A0 (fi)
NO (1)	NO843148L (fi)
NZ (1)	NZ206596A (fi)
WO (1)	WO1984002339A1 (fi)
ZA (1)	ZA839343B (fi)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8415150D0 (en) *	1984-06-14	1984-07-18	British Petroleum Co Plc	Coproduction of dialkyl carbonate/dialkyl and tertiary butanol
GB8415807D0 (en) *	1984-06-21	1984-07-25	British Petroleum Co Plc	Oxidative carbonylation catalysts
EP0217651A3 (en) *	1985-09-30	1988-11-17	Texaco Development Corporation	Preparation of organic carbonates
GB8526306D0 (en) *	1985-10-24	1985-11-27	British Petroleum Co Plc	Carbonate esters
EP0474342A1 (en) *	1990-09-05	1992-03-11	ARCO Chemical Technology, L.P.	Unsymmetrical dialkyl carbonate fuel additives
EP3399008B1 (de) *	2017-05-02	2020-03-18	ASG Analytik-Service Gesellschaft mbH	Potenziell co2-neutraler und umweltschonender ottokraftstoff auf basis der c1-chemie

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3016187A1 (de) *	1980-04-26	1981-10-29	Bayer Ag	Verfahren zur herstellung von kohlensaeureestern

1983
- 1983-12-14 CA CA000443293A patent/CA1218670A/en not_active Expired
- 1983-12-15 AU AU23450/84A patent/AU570941B2/en not_active Ceased
- 1983-12-15 DE DE8383307633T patent/DE3372858D1/de not_active Expired
- 1983-12-15 EP EP83307633A patent/EP0112172B1/en not_active Expired
- 1983-12-15 NZ NZ206596A patent/NZ206596A/en unknown
- 1983-12-15 ZA ZA839343A patent/ZA839343B/xx unknown
- 1983-12-15 WO PCT/GB1983/000335 patent/WO1984002339A1/en active Application Filing
- 1983-12-15 JP JP84500271A patent/JPS60500259A/ja active Pending
1984
- 1984-08-06 NO NO843148A patent/NO843148L/no unknown
- 1984-08-09 FI FI843139A patent/FI843139A0/fi not_active Application Discontinuation

Also Published As

Publication number	Publication date
JPS60500259A (ja)	1985-02-28
DE3372858D1 (en)	1987-09-10
AU570941B2 (en)	1988-03-31
CA1218670A (en)	1987-03-03
EP0112172A1 (en)	1984-06-27
AU2345084A (en)	1984-07-05
NZ206596A (en)	1985-12-13
EP0112172B1 (en)	1987-08-05
ZA839343B (en)	1985-07-31
FI843139A (fi)	1984-08-09
WO1984002339A1 (en)	1984-06-21
FI843139A0 (fi)	1984-08-09

Publication	Publication Date	Title
US4045464A (en)	1977-08-30	Process for the preparation of aromatic carbonates
US4002678A (en)	1977-01-11	Preparation of carboxylic acid anhydrides
Alper et al.	1987	Conversion of primary amines to carbamate esters using palladium chloride and di-tert-butyl peroxide. Double carbonylation of secondary amines
US2727902A (en)	1955-12-20	Process for the production of aliphatic oxygen compounds by carbonylation of alcohols and ethers
US3028417A (en)	1962-04-03	Process of making hydroxy ester compounds
US4002677A (en)	1977-01-11	Process for preparing carboxylic acid anhydrides
EP0639559B1 (en)	1997-10-15	Preparation of 1,2-diacyl-2-(t-alkyl)hydrazines
US4356320A (en)	1982-10-26	Preparation of carboxylic acids
NO843148L (no)	1984-08-06	Fremgangsmaate for fremstilling av dihydrokarbylkarbonater, deres anvendelse som drivstoff-tilsetninger og drivstoffsammensetninger inneholdende disse
Padias et al.	1981	Oligomeric bishydroxybutyl terephthalates from terephthalic acid
EP0463678A2 (en)	1992-01-02	Process and catalyst for preparing organic carbonates
GB1567594A (en)	1980-05-21	Process for preparing carboxylic acids
KR101632449B1 (ko)	2016-06-21	알콕시카보닐 화합물의 제조 방법
US4894474A (en)	1990-01-16	Preparation of alkyl pentenoates
US4284585A (en)	1981-08-18	Process for the preparation of acetic anhydride
EP0163442B1 (en)	1988-10-19	Process for the preparation of esters of dicarboxylic acids
US4431593A (en)	1984-02-14	Ester preparation by carbonylation of monoolefins
CA1105060A (en)	1981-07-14	Hydrocarbonylation of methanol to ethanol in the presence of added compounds
US5756824A (en)	1998-05-26	Process for the preparation of carbazates
US4521614A (en)	1985-06-04	Carbonylation of monoolefins
KR101898362B1 (ko)	2018-09-12	(메트)아크릴산 에스터의 제조 방법 및 카복실산 방향족 에스터의 제조 방법
US4284586A (en)	1981-08-18	Process for the preparation of acetic anhydride
AU558487B2 (en)	1987-01-29	Process for the production of dihydrocarbyl oxalates
JPH0127056B2 (fi)	1989-05-26
US4816595A (en)	1989-03-28	Preparation of carbonate esters