RU2000117273A - CATALYSTS ETERIFICATION - Google Patents
CATALYSTS ETERIFICATIONInfo
- Publication number
- RU2000117273A RU2000117273A RU2000117273/04A RU2000117273A RU2000117273A RU 2000117273 A RU2000117273 A RU 2000117273A RU 2000117273/04 A RU2000117273/04 A RU 2000117273/04A RU 2000117273 A RU2000117273 A RU 2000117273A RU 2000117273 A RU2000117273 A RU 2000117273A
- Authority
- RU
- Russia
- Prior art keywords
- acid
- organometallic catalyst
- catalyst according
- zirconium
- titanium
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims 18
- 125000002524 organometallic group Chemical group 0.000 claims 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 10
- RTAQQCXQSZGOHL-UHFFFAOYSA-N titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 10
- 229910052719 titanium Inorganic materials 0.000 claims 10
- 239000010936 titanium Substances 0.000 claims 10
- QCWXUUIWCKQGHC-UHFFFAOYSA-N zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims 10
- 229910052726 zirconium Inorganic materials 0.000 claims 10
- 229910052782 aluminium Inorganic materials 0.000 claims 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 8
- 238000005886 esterification reaction Methods 0.000 claims 7
- 150000002903 organophosphorus compounds Chemical class 0.000 claims 7
- 239000010452 phosphate Substances 0.000 claims 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 6
- 150000002148 esters Chemical class 0.000 claims 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 6
- -1 aluminum ortho ester Chemical class 0.000 claims 5
- 238000006243 chemical reaction Methods 0.000 claims 5
- WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-Butanediol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 125000004432 carbon atoms Chemical group C* 0.000 claims 4
- 150000002905 orthoesters Chemical class 0.000 claims 4
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 2
- SECPZKHBENQXJG-FPLPWBNLSA-N Palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 claims 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims 2
- 239000007795 chemical reaction product Substances 0.000 claims 2
- 239000000047 product Substances 0.000 claims 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (-)-propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N 1,6-Hexanediol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims 1
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-Methyl-2,4-pentanediol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims 1
- WTDBQJMMOXGIQZ-UHFFFAOYSA-N 3,4-dimethylnaphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=C2C(C(O)=O)=C(C(O)=O)C(C)=C(C)C2=C1 WTDBQJMMOXGIQZ-UHFFFAOYSA-N 0.000 claims 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N Azelaic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims 1
- 239000005711 Benzoic acid Substances 0.000 claims 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 claims 1
- WOZVHXUHUFLZGK-UHFFFAOYSA-N Dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 claims 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N Hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims 1
- 229960000448 Lactic acid Drugs 0.000 claims 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N Malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims 1
- VHOCUJPBKOZGJD-UHFFFAOYSA-N Melissic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O VHOCUJPBKOZGJD-UHFFFAOYSA-N 0.000 claims 1
- FEWJPZIEWOKRBE-XIXRPRMCSA-N Mesotartaric acid Chemical compound OC(=O)[C@@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-XIXRPRMCSA-N 0.000 claims 1
- 235000021319 Palmitoleic acid Nutrition 0.000 claims 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N Phosphite Chemical compound [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims 1
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 229960004063 Propylene glycol Drugs 0.000 claims 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J Pyrophosphate Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 claims 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- ATMLPEJAVWINOF-UHFFFAOYSA-N acrylic acid acrylic acid Chemical compound OC(=O)C=C.OC(=O)C=C ATMLPEJAVWINOF-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 229920002892 amber Polymers 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 235000010233 benzoic acid Nutrition 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 229960004106 citric acid Drugs 0.000 claims 1
- 235000015165 citric acid Nutrition 0.000 claims 1
- 235000011180 diphosphates Nutrition 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 1
- 235000011187 glycerol Nutrition 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims 1
- 239000004310 lactic acid Substances 0.000 claims 1
- 235000014655 lactic acid Nutrition 0.000 claims 1
- 239000001630 malic acid Substances 0.000 claims 1
- 229940099690 malic acid Drugs 0.000 claims 1
- 235000011090 malic acid Nutrition 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 claims 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims 1
- NJRWNWYFPOFDFN-UHFFFAOYSA-L phosphonate(2-) Chemical compound [O-][P]([O-])=O NJRWNWYFPOFDFN-UHFFFAOYSA-L 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 235000013772 propylene glycol Nutrition 0.000 claims 1
- 239000011975 tartaric acid Substances 0.000 claims 1
- 229960001367 tartaric acid Drugs 0.000 claims 1
- 235000002906 tartaric acid Nutrition 0.000 claims 1
Claims (22)
(a) сложного ортоэфира или конденсированного сложного ортоэфира титана, циркония или алюминия,
(b) спирта, содержащего, по меньшей мере, две гидроксильные группы,
(c) фосфорорганического соединения, содержащего, по меньшей мере, одну группу Р-ОН и
(d) основания
путем смешения вышеуказанных компонентов.1. ORGANOMETALLIC Catalyst for the preparation of an ester comprising the reaction product involving the interaction
(a) an ortho ester or a condensed titanium, zirconium or aluminum ortho ester,
(b) an alcohol containing at least two hydroxyl groups,
(c) an organophosphorus compound containing at least one P-OH group and
(d) grounds
by mixing the above components.
(a) сложного ортоэфира или конденсированного сложного ортоэфира титана, циркония или алюминия,
(b) спирта, содержащего, по меньшей мере, две гидроксильные группы,
(c) фосфорорганического соединения, содержащего, по меньшей мере, одну группу Р-ОН и
(d) основания.15. A method of producing an ester, comprising performing an esterification reaction in the presence of an organometallic catalyst comprising the reaction product
(a) an ortho ester or a condensed titanium, zirconium or aluminum ortho ester,
(b) an alcohol containing at least two hydroxyl groups,
(c) an organophosphorus compound containing at least one P-OH group and
(d) grounds.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9725419.7 | 1997-12-02 | ||
GBGB9725419.7A GB9725419D0 (en) | 1997-12-02 | 1997-12-02 | Esterification catalysts |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2181307C2 RU2181307C2 (en) | 2002-04-20 |
RU2000117273A true RU2000117273A (en) | 2002-07-10 |
Family
ID=10822947
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000117273/04A RU2181307C2 (en) | 1997-12-02 | 1998-11-16 | Esterification catalysts |
Country Status (25)
Country | Link |
---|---|
US (1) | US6372929B1 (en) |
EP (1) | EP1035916B1 (en) |
JP (1) | JP4377053B2 (en) |
KR (1) | KR100552882B1 (en) |
CN (1) | CN1167508C (en) |
AR (1) | AR017422A1 (en) |
AT (1) | ATE205114T1 (en) |
AU (1) | AU746951B2 (en) |
BR (1) | BR9814709A (en) |
CA (1) | CA2309697A1 (en) |
CO (1) | CO4810385A1 (en) |
DE (1) | DE69801596T2 (en) |
ES (1) | ES2162478T3 (en) |
GB (1) | GB9725419D0 (en) |
HU (1) | HUP0004493A3 (en) |
ID (1) | ID24715A (en) |
MY (1) | MY128075A (en) |
NO (1) | NO20002782L (en) |
NZ (1) | NZ504219A (en) |
PL (1) | PL192913B1 (en) |
RU (1) | RU2181307C2 (en) |
SK (1) | SK8312000A3 (en) |
TR (1) | TR200001539T2 (en) |
TW (1) | TW448073B (en) |
WO (1) | WO1999028033A1 (en) |
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US5453479A (en) * | 1993-07-12 | 1995-09-26 | General Electric Company | Polyesterification catalyst |
DE19518943C2 (en) * | 1995-05-23 | 1999-12-09 | Inventa Fischer Gmbh | Process for the production of polyesters using titanium-containing catalyst-inhibitor combinations |
GB2314081B (en) * | 1996-06-11 | 2000-02-23 | Tioxide Specialties Ltd | Esterification process using an organotitanium or organozirconium catalyst |
EP0816354A1 (en) * | 1996-06-25 | 1998-01-07 | Bayer Ag | Process for preparing and stabilisation of aliphatic six-membered cyclic carbonates |
-
1997
- 1997-12-02 GB GBGB9725419.7A patent/GB9725419D0/en not_active Ceased
-
1998
- 1998-11-16 AT AT98954609T patent/ATE205114T1/en not_active IP Right Cessation
- 1998-11-16 WO PCT/GB1998/003448 patent/WO1999028033A1/en active IP Right Grant
- 1998-11-16 JP JP2000523004A patent/JP4377053B2/en not_active Expired - Lifetime
- 1998-11-16 CN CNB988117010A patent/CN1167508C/en not_active Expired - Lifetime
- 1998-11-16 KR KR1020007005951A patent/KR100552882B1/en not_active IP Right Cessation
- 1998-11-16 AU AU11664/99A patent/AU746951B2/en not_active Ceased
- 1998-11-16 DE DE69801596T patent/DE69801596T2/en not_active Expired - Lifetime
- 1998-11-16 RU RU2000117273/04A patent/RU2181307C2/en not_active IP Right Cessation
- 1998-11-16 BR BR9814709-9A patent/BR9814709A/en not_active Application Discontinuation
- 1998-11-16 PL PL340912A patent/PL192913B1/en unknown
- 1998-11-16 HU HU0004493A patent/HUP0004493A3/en unknown
- 1998-11-16 ES ES98954609T patent/ES2162478T3/en not_active Expired - Lifetime
- 1998-11-16 SK SK831-2000A patent/SK8312000A3/en unknown
- 1998-11-16 ID IDW20001038A patent/ID24715A/en unknown
- 1998-11-16 TR TR2000/01539T patent/TR200001539T2/en unknown
- 1998-11-16 CA CA002309697A patent/CA2309697A1/en not_active Abandoned
- 1998-11-16 NZ NZ504219A patent/NZ504219A/en unknown
- 1998-11-16 EP EP98954609A patent/EP1035916B1/en not_active Expired - Lifetime
- 1998-11-27 TW TW087119733A patent/TW448073B/en not_active IP Right Cessation
- 1998-11-30 CO CO98070685A patent/CO4810385A1/en unknown
- 1998-11-30 MY MYPI98005421A patent/MY128075A/en unknown
- 1998-12-01 AR ARP980106093A patent/AR017422A1/en active IP Right Grant
-
2000
- 2000-05-09 US US09/568,206 patent/US6372929B1/en not_active Expired - Lifetime
- 2000-05-31 NO NO20002782A patent/NO20002782L/en not_active Application Discontinuation
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