ES2060973T3 - Procedimiento de fabricacion de cloruro de acriloilo. - Google Patents
Procedimiento de fabricacion de cloruro de acriloilo.Info
- Publication number
- ES2060973T3 ES2060973T3 ES90400453T ES90400453T ES2060973T3 ES 2060973 T3 ES2060973 T3 ES 2060973T3 ES 90400453 T ES90400453 T ES 90400453T ES 90400453 T ES90400453 T ES 90400453T ES 2060973 T3 ES2060973 T3 ES 2060973T3
- Authority
- ES
- Spain
- Prior art keywords
- catalyst
- acrylic acid
- acryloyl chloride
- procedure
- manufacture
- 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.)
- Expired - Lifetime
Links
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 3
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- XEMRAKSQROQPBR-UHFFFAOYSA-N (trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=CC=C1 XEMRAKSQROQPBR-UHFFFAOYSA-N 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 239000002841 Lewis acid Substances 0.000 abstract 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 150000007517 lewis acids Chemical class 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 239000011787 zinc oxide Substances 0.000 abstract 1
- 229910052726 zirconium Inorganic materials 0.000 abstract 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
- 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
EL CLORURO DE ACRILOILO SE OBTIENE POR REACCION DEL ACIDO ACRILICO CON FENILCLOROFORMO, EN PRESENCIA DE UN ACIDO DE LEWIS POR LO MENOS COMO CATALIZADOR Y POR LO MENOS UN AGENTE INHIBIDOR DE POLIMERACION. SEGUN LA INVENCION, EL CATALIZADOR SE ELIGE ENTRE OXIDO DE CINC Y TETRACLORURO DE CIRCONIO Y SE EFECTUA LA REACCION A UNA TEMPERATURA DE POR LO MENOS 105 (GRADOS) C. EN UNA FORMA DE REALIZACION PREFERIDA, SE AÑADE EL ACIDO ACRILICO AL MEDIO CONSTITUIDO POR FENILCLOROFORMO, EL CATALIZADOR Y EL INHIBIDOR DE POLIMERIZACION, Y SE LLEVA A UNA TEMPERATURA DE POR LO MENOS 105 (GRADOS) C, DESTILANDO EL CLORURO DE ACRILOILO FORMADO DESDE LA PRIMERA INTRODUCCION DEL ACIDO ACRILICO. EL CLORURO DE ACRILOILO ES UN INTERMEDIO DE SINTESIS MUY REACTIVO
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8902918A FR2643901B1 (fr) | 1989-03-06 | 1989-03-06 | Procede de fabrication de chlorure d'acryloyle |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2060973T3 true ES2060973T3 (es) | 1994-12-01 |
Family
ID=9379411
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES90400453T Expired - Lifetime ES2060973T3 (es) | 1989-03-06 | 1990-02-19 | Procedimiento de fabricacion de cloruro de acriloilo. |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0387116B1 (es) |
| JP (1) | JPH04502765A (es) |
| AT (1) | ATE98212T1 (es) |
| CA (1) | CA2028831C (es) |
| DD (1) | DD295625A5 (es) |
| DE (1) | DE69005000T2 (es) |
| DK (1) | DK0387116T3 (es) |
| ES (1) | ES2060973T3 (es) |
| FR (1) | FR2643901B1 (es) |
| WO (1) | WO1990010616A1 (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0813764A2 (pt) * | 2007-06-28 | 2014-12-30 | 3M Innovative Properties Co | Processo para formação de haletos de carbonila alfa, beta-insaturados |
| CN109553526B (zh) * | 2018-12-18 | 2022-07-05 | 杭州盛弗泰新材料科技有限公司 | 一种丙烯酰氯的连续生产方法 |
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 (de) * | 1984-06-18 | 1985-12-19 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung halogenierter aliphatischer carbonsaeurefluoride |
-
1989
- 1989-03-06 FR FR8902918A patent/FR2643901B1/fr not_active Expired - Fee Related
-
1990
- 1990-01-18 JP JP2502634A patent/JPH04502765A/ja active Pending
- 1990-01-18 WO PCT/FR1990/000040 patent/WO1990010616A1/fr not_active Ceased
- 1990-01-18 CA CA002028831A patent/CA2028831C/fr not_active Expired - Fee Related
- 1990-02-19 AT AT90400453T patent/ATE98212T1/de not_active IP Right Cessation
- 1990-02-19 EP EP90400453A patent/EP0387116B1/fr not_active Expired - Lifetime
- 1990-02-19 DK DK90400453.8T patent/DK0387116T3/da active
- 1990-02-19 DE DE90400453T patent/DE69005000T2/de not_active Expired - Fee Related
- 1990-02-19 ES ES90400453T patent/ES2060973T3/es not_active Expired - Lifetime
- 1990-07-24 DD DD90343020A patent/DD295625A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| ATE98212T1 (de) | 1993-12-15 |
| WO1990010616A1 (fr) | 1990-09-20 |
| CA2028831A1 (fr) | 1990-09-07 |
| JPH04502765A (ja) | 1992-05-21 |
| EP0387116B1 (fr) | 1993-12-08 |
| FR2643901B1 (fr) | 1991-09-06 |
| DD295625A5 (de) | 1991-11-07 |
| DE69005000D1 (de) | 1994-01-20 |
| EP0387116A1 (fr) | 1990-09-12 |
| DE69005000T2 (de) | 1994-04-28 |
| FR2643901A1 (fr) | 1990-09-07 |
| DK0387116T3 (da) | 1994-02-14 |
| CA2028831C (fr) | 1997-05-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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