JPS6024088B2 - フッ化イソブチリルの製造方法 - Google Patents

フッ化イソブチリルの製造方法

Info

Publication number: JPS6024088B2
Authority: JP; Japan
Prior art keywords: propylene; carbon monoxide; pressure; rate; fluoride
Prior art date: 1981-06-29
Legal status (The legal status 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 status listed.): Expired

Application number

JP57096065A

Other languages

English (en)

Japanese (ja)

Other versions

JPS588036A (ja

Inventor

ブ−ペンドラ・シ−・トリベデイ

デイス・グロウト

ト−マス・オ−・メイスン

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Ashland LLC

Original Assignee

Ashland Oil Inc

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.)

1981-06-29

Filing date

1982-06-04

Publication date

1985-06-11

1982-06-04 Application filed by Ashland Oil Inc filed Critical Ashland Oil Inc

1983-01-18 Publication of JPS588036A publication Critical patent/JPS588036A/ja

1985-06-11 Publication of JPS6024088B2 publication Critical patent/JPS6024088B2/ja

Status Expired legal-status Critical Current

Links

FSQOYWQCIXSBNP-UHFFFAOYSA-N 2-methylpropanoyl fluoride Chemical compound CC(C)C(F)=O FSQOYWQCIXSBNP-UHFFFAOYSA-N 0.000 title claims description 21
238000004519 manufacturing process Methods 0.000 title claims description 5
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 67
229910002091 carbon monoxide Inorganic materials 0.000 claims description 67
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 59
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 59
239000012071 phase Substances 0.000 claims description 20
239000011541 reaction mixture Substances 0.000 claims description 15
239000007791 liquid phase Substances 0.000 claims description 13
150000008064 anhydrides Chemical class 0.000 claims description 12
238000000034 method Methods 0.000 claims description 11
239000007788 liquid Substances 0.000 claims description 10
239000012530 fluid Substances 0.000 claims description 7
239000000463 material Substances 0.000 claims 1
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 27
238000006243 chemical reaction Methods 0.000 description 20
239000000203 mixture Substances 0.000 description 18
239000000047 product Substances 0.000 description 17
239000007789 gas Substances 0.000 description 12
229910000040 hydrogen fluoride Inorganic materials 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
150000008065 acid anhydrides Chemical class 0.000 description 7
150000001450 anions Chemical class 0.000 description 7
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 6
238000005810 carbonylation reaction Methods 0.000 description 5
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
150000001336 alkenes Chemical class 0.000 description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
150000001733 carboxylic acid esters Chemical class 0.000 description 4
KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
239000002253 acid Substances 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
230000006315 carbonylation Effects 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
238000000926 separation method Methods 0.000 description 3
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
238000001816 cooling Methods 0.000 description 2
238000004821 distillation Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
BHIWKHZACMWKOJ-UHFFFAOYSA-N methyl isobutyrate Chemical compound COC(=O)C(C)C BHIWKHZACMWKOJ-UHFFFAOYSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
150000002894 organic compounds Chemical class 0.000 description 2
239000001294 propane Substances 0.000 description 2
BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
238000007086 side reaction Methods 0.000 description 2
239000000243 solution Substances 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
206010067482 No adverse event Diseases 0.000 description 1
101100227721 Rattus norvegicus Frk gene Proteins 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
239000011260 aqueous acid Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
RBHJBMIOOPYDBQ-UHFFFAOYSA-N carbon dioxide;propan-2-one Chemical compound O=C=O.CC(C)=O RBHJBMIOOPYDBQ-UHFFFAOYSA-N 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
239000000284 extract Substances 0.000 description 1
238000000605 extraction Methods 0.000 description 1
GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
150000002222 fluorine compounds Chemical class 0.000 description 1
229910000856 hastalloy Inorganic materials 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
239000005457 ice water Substances 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
230000002427 irreversible effect Effects 0.000 description 1
WDAXFOBOLVPGLV-UHFFFAOYSA-N isobutyric acid ethyl ester Natural products CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 description 1
-1 methyl isobutyrate Chemical class 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
- C07C51/14—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on a carbon-to-carbon unsaturated bond in organic compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
- C07C51/12—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on an oxygen-containing group in organic compounds, e.g. alcohols
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/36—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates
- C07C67/38—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates by addition to an unsaturated carbon-to-carbon bond
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/54—Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP57096065A 1981-06-29 1982-06-04 フッ化イソブチリルの製造方法 Expired JPS6024088B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US27876481A	1981-06-29	1981-06-29
US278764		1981-06-29

Publications (2)

Publication Number	Publication Date
JPS588036A JPS588036A (ja)	1983-01-18
JPS6024088B2 true JPS6024088B2 (ja)	1985-06-11

Family

ID=23066263

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP57096065A Expired JPS6024088B2 (ja)	1981-06-29	1982-06-04	フッ化イソブチリルの製造方法

Country Status (12)

Country	Link
JP (1)	JPS6024088B2 (it)
KR (1)	KR850001914B1 (it)
AT (1)	AT388160B (it)
AU (1)	AU532639B2 (it)
BE (1)	BE893419A (it)
CA (1)	CA1173057A (it)
CH (1)	CH660180A5 (it)
DE (1)	DE3221172C2 (it)
FR (1)	FR2508441B1 (it)
GB (1)	GB2100729B (it)
IT (1)	IT1195930B (it)
NL (1)	NL187013C (it)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NZ195559A (en) *	1979-11-29	1984-03-16	Ris Irrigation Syst	Butterfly sprinkler with dust protection for bearing
US4499029A (en) *	1983-06-15	1985-02-12	Ashland Oil, Inc.	Isobutyryl fluoride manufacture
DE3725428A1 (de) *	1987-07-31	1989-02-09	Basf Ag	Verfahren zur herstellung von carbonsaeurehalogeniden
FR2691965A1 (fr) *	1992-06-04	1993-12-10	Atochem Elf Sa	Procédé de fabrication de fluorure d'isobutyryle.
GB9917429D0 (en) *	1999-07-23	1999-09-22	Swan Thomas & Co Ltd	Carbonylation reactions

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE972291C (de) *	1954-05-16	1959-07-02	Studiengesellschaft Kohle Mbh	Verfahren zur Herstellung von Monocarbonsaeuren aus Olefinen, Kohlenoxyd und Wasser
DE973077C (de) *	1954-07-30	1959-11-26	Studiengesellschaft Kohle Mbh	Verfahren zur Herstellung von Carbonsaeuren aus Olefinen und Kohlenoxyd
DE1064941B (de) *	1957-04-24	1959-09-10	Studiengesellschaft Kohle Mbh	Verfahren zur Herstellung von Gemischen aus gesaettigten aliphatischen oder cycloaliphatischen Monocarbonsaeurealkylestern
US3065242A (en) *	1960-02-23	1962-11-20	Du Pont	Production of acyl halides, carboxylic acids and lactones
US3167585A (en) *	1960-08-25	1965-01-26	Gulf Research Development Co	Process for carboxylation of iso-olefins
GB942367A (en) *	1961-04-29	1963-11-20	Basf Ag	Continuous production of carboxylic acids from olefines, carbon monoxide and water
NL6816940A (it) *	1967-11-28	1969-05-30
GB1232317A (it) *	1968-12-30	1971-05-19
BE755997A (fr) *	1969-09-11	1971-03-10	Bp Chem Int Ltd	Production d'acides dicarboxyliques
DE2750719A1 (de) *	1977-11-12	1979-05-17	Roehm Gmbh	Verfahren zur herstellung von isobuttersaeure
US4224232A (en) *	1978-12-21	1980-09-23	Gulf Research & Development Company	Production of carboxylic acids from olefins and mixtures of olefins
EP0017441B2 (en) *	1979-04-09	1987-10-28	CHEM SYSTEMS, Inc.	Preparation of esters

1982
- 1982-06-03 AT AT0215082A patent/AT388160B/de not_active IP Right Cessation
- 1982-06-04 FR FR8209809A patent/FR2508441B1/fr not_active Expired
- 1982-06-04 CH CH3476/82A patent/CH660180A5/de not_active IP Right Cessation
- 1982-06-04 IT IT21707/82A patent/IT1195930B/it active
- 1982-06-04 NL NLAANVRAGE8202268,A patent/NL187013C/xx not_active IP Right Cessation
- 1982-06-04 JP JP57096065A patent/JPS6024088B2/ja not_active Expired
- 1982-06-04 DE DE3221172A patent/DE3221172C2/de not_active Expired
- 1982-06-04 CA CA000404487A patent/CA1173057A/en not_active Expired
- 1982-06-04 BE BE0/208271A patent/BE893419A/fr not_active IP Right Cessation
- 1982-06-04 AU AU84609/82A patent/AU532639B2/en not_active Ceased
- 1982-06-04 KR KR8202507A patent/KR850001914B1/ko active
- 1982-06-04 GB GB08216304A patent/GB2100729B/en not_active Expired

Also Published As

Publication number	Publication date
NL8202268A (nl)	1983-01-17
KR840000461A (ko)	1984-02-22
GB2100729B (en)	1985-10-30
GB2100729A (en)	1983-01-06
KR850001914B1 (ko)	1985-12-31
FR2508441B1 (fr)	1987-04-30
AU8460982A (en)	1983-03-10
ATA215082A (de)	1988-10-15
AT388160B (de)	1989-05-10
NL187013C (nl)	1991-05-01
DE3221172C2 (de)	1984-08-02
DE3221172A1 (de)	1983-01-05
IT8221707A0 (it)	1982-06-04
FR2508441A1 (fr)	1982-12-31
CA1173057A (en)	1984-08-21
CH660180A5 (de)	1987-03-31
NL187013B (nl)	1990-12-03
IT1195930B (it)	1988-11-03
BE893419A (fr)	1982-10-01
JPS588036A (ja)	1983-01-18
AU532639B2 (en)	1983-10-06

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US2152852A (en)	1939-04-04	Process for manufacture of glycolic acid
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US20080269459A1 (en)	2008-10-30	Process for the Preparation of a Dicarboxylic Acid
JPS6024088B2 (ja)	1985-06-11	フッ化イソブチリルの製造方法
TWI744336B (zh)	2021-11-01	製程
US5087757A (en)	1992-02-11	Preparation of alkylthioethylamine salts
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CA2093749C (en)	1999-06-22	Process for preparing ethylidene diacetate using iodine catalysts
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US4408080A (en)	1983-10-04	Process for producing acetaldehyde
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