CA2028831A1 - Process for the fabrication of acryloyl chloride - Google Patents
Process for the fabrication of acryloyl chlorideInfo
- Publication number
- CA2028831A1 CA2028831A1 CA2028831A CA2028831A CA2028831A1 CA 2028831 A1 CA2028831 A1 CA 2028831A1 CA 2028831 A CA2028831 A CA 2028831A CA 2028831 A CA2028831 A CA 2028831A CA 2028831 A1 CA2028831 A1 CA 2028831A1
- Authority
- CA
- Canada
- Prior art keywords
- acryloyl chloride
- catalyst
- acrylic acid
- fabrication
- phenylchloroform
- Prior art date
- 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.)
- Granted
Links
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
- C07C51/60—Preparation of carboxylic acid halides by conversion of carboxylic acids or their anhydrides or esters, lactones, salts into halides with the same carboxylic acid part
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Acryloyl chloride is obtained by the reaction of acrylic acid on phenylchloroform, in the presence of at least one Lewis acid as catalyst and at least one polymerisation inhibiting agent. According to the invention, the catalyst is chosen among zinc oxide and zirconium tetrchloride and the reaction is brought to a temperature of at least 105 DEG C. In a preferred embodiment, the acrylic acid is added to the medium consisting of phenylchloroform, the catalyst and the polymerization inhibitor, and brought to a temperature of at least 105 DEG C, whereby the acryloyl chloride formed distils as soon as the acrylic acid is introduced. Acryloyl chloride is a highly reactive synthesis intermediate.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR89/02918 | 1989-03-06 | ||
FR8902918A FR2643901B1 (en) | 1989-03-06 | 1989-03-06 | PROCESS FOR THE MANUFACTURE OF ACRYLOYL CHLORIDE |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2028831A1 true CA2028831A1 (en) | 1990-09-07 |
CA2028831C CA2028831C (en) | 1997-05-20 |
Family
ID=9379411
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002028831A Expired - Fee Related CA2028831C (en) | 1989-03-06 | 1990-01-18 | Process for the fabrication of acryloyl chloride |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0387116B1 (en) |
JP (1) | JPH04502765A (en) |
AT (1) | ATE98212T1 (en) |
CA (1) | CA2028831C (en) |
DD (1) | DD295625A5 (en) |
DE (1) | DE69005000T2 (en) |
DK (1) | DK0387116T3 (en) |
ES (1) | ES2060973T3 (en) |
FR (1) | FR2643901B1 (en) |
WO (1) | WO1990010616A1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20100044186A (en) * | 2007-06-28 | 2010-04-29 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | Process for forming alpha, beta-unsaturated carbonyl halides |
CN109553526B (en) * | 2018-12-18 | 2022-07-05 | 杭州盛弗泰新材料科技有限公司 | Continuous production method of acryloyl chloride |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1921767A (en) * | 1929-05-20 | 1933-08-08 | Dow Chemical Co | Method of making acid halides |
US1963749A (en) * | 1932-07-30 | 1934-06-19 | Monsanto Chemicals | Manufacture of aromatic dicarboxylic acid chlorides |
DE3422576A1 (en) * | 1984-06-18 | 1985-12-19 | Hoechst Ag, 6230 Frankfurt | METHOD FOR PRODUCING HALOGENATED ALIPHATIC CARBONIC ACID FLUORIDES |
-
1989
- 1989-03-06 FR FR8902918A patent/FR2643901B1/en not_active Expired - Fee Related
-
1990
- 1990-01-18 JP JP2502634A patent/JPH04502765A/en active Pending
- 1990-01-18 CA CA002028831A patent/CA2028831C/en not_active Expired - Fee Related
- 1990-01-18 WO PCT/FR1990/000040 patent/WO1990010616A1/en active Application Filing
- 1990-02-19 DK DK90400453.8T patent/DK0387116T3/en active
- 1990-02-19 AT AT90400453T patent/ATE98212T1/en not_active IP Right Cessation
- 1990-02-19 ES ES90400453T patent/ES2060973T3/en not_active Expired - Lifetime
- 1990-02-19 EP EP90400453A patent/EP0387116B1/en not_active Expired - Lifetime
- 1990-02-19 DE DE90400453T patent/DE69005000T2/en not_active Expired - Fee Related
- 1990-07-24 DD DD90343020A patent/DD295625A5/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE69005000T2 (en) | 1994-04-28 |
FR2643901A1 (en) | 1990-09-07 |
FR2643901B1 (en) | 1991-09-06 |
ES2060973T3 (en) | 1994-12-01 |
DD295625A5 (en) | 1991-11-07 |
DK0387116T3 (en) | 1994-02-14 |
EP0387116A1 (en) | 1990-09-12 |
EP0387116B1 (en) | 1993-12-08 |
JPH04502765A (en) | 1992-05-21 |
ATE98212T1 (en) | 1993-12-15 |
DE69005000D1 (en) | 1994-01-20 |
WO1990010616A1 (en) | 1990-09-20 |
CA2028831C (en) | 1997-05-20 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKLA | Lapsed |