JPS5540613A - Preparation of 2, 6-dichloro-4-alkylphenol - Google Patents
Preparation of 2, 6-dichloro-4-alkylphenolInfo
- Publication number
- JPS5540613A JPS5540613A JP11309078A JP11309078A JPS5540613A JP S5540613 A JPS5540613 A JP S5540613A JP 11309078 A JP11309078 A JP 11309078A JP 11309078 A JP11309078 A JP 11309078A JP S5540613 A JPS5540613 A JP S5540613A
- Authority
- JP
- Japan
- Prior art keywords
- alkylphenol
- amount
- amines
- solvent
- catalyst
- 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
-
- 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
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PURPOSE: To obtain the high purity title compound, useful as a synthetic intermediate of, e.g. agricultural chemicals, in high yield, by reacting 4-alkylphenol with Cl2 in a solvent in the presence of an amine as a catalyst, thereby chlorinating the alkylphenol at the nucleus.
CONSTITUTION: 4-Alkylphenol of the formula (R=lower alkyl) and Cl2 are introduced simultaneously into a reaction vessel containing a specific amount of a slvent, e.g. tetrachlorethylene, and a specific amount of a catalyst of amines. The nucleic chlorination is accomplished at 0W90°C for 1W20hr. After washing the reaction products with n aqueous solution of e.g. Na2SO3, the solvent is removed to give the objective compound. The amines used are e.g. dicyclohexylamine, n-propylamine, aniline, benzylamine, morpholine etc. The amount of these amines is 0.0001W0.003mol to 1mol of 4-alkylphenol. The amount of the solvent used is 1-several times the amount of 4-alkylphenol.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11309078A JPS5540613A (en) | 1978-09-14 | 1978-09-14 | Preparation of 2, 6-dichloro-4-alkylphenol |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11309078A JPS5540613A (en) | 1978-09-14 | 1978-09-14 | Preparation of 2, 6-dichloro-4-alkylphenol |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5540613A true JPS5540613A (en) | 1980-03-22 |
| JPS5630332B2 JPS5630332B2 (en) | 1981-07-14 |
Family
ID=14603218
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11309078A Granted JPS5540613A (en) | 1978-09-14 | 1978-09-14 | Preparation of 2, 6-dichloro-4-alkylphenol |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5540613A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4503214A (en) * | 1983-12-05 | 1985-03-05 | General Electric Company | Continuous process for preparing polyphenylene oxides |
| FR2578836A1 (en) * | 1985-03-12 | 1986-09-19 | Rhone Poulenc Spec Chim | METHOD FOR SELECTIVE CHLORINATION OF PHENOLIC COMPOUNDS |
| FR2587332A1 (en) * | 1985-09-19 | 1987-03-20 | Rhone Poulenc Spec Chim | METHOD FOR SELECTIVE CHLORINATION OF PHENOLIC COMPOUNDS |
| JPS63238025A (en) * | 1987-03-05 | 1988-10-04 | ローヌ−.プーラン・シミ | Chlorination of phenol compound |
| CN1035324C (en) * | 1995-02-16 | 1997-07-02 | 建湖县有机化工厂 | Process for production of 2,6-dichlorophenol by using O-chlorophenol |
| US6635787B2 (en) | 2001-12-20 | 2003-10-21 | Sumitomo Chemical Company, Limited | Production method of a 2,6-dichlorophenol compound |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS601143U (en) * | 1983-06-18 | 1985-01-07 | 株式会社 ノ−リツ研究センタ− | paper mask device |
| KR101725920B1 (en) * | 2016-12-22 | 2017-04-11 | (주) 드림 | Ignition coil body automatic production device |
-
1978
- 1978-09-14 JP JP11309078A patent/JPS5540613A/en active Granted
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4503214A (en) * | 1983-12-05 | 1985-03-05 | General Electric Company | Continuous process for preparing polyphenylene oxides |
| FR2578836A1 (en) * | 1985-03-12 | 1986-09-19 | Rhone Poulenc Spec Chim | METHOD FOR SELECTIVE CHLORINATION OF PHENOLIC COMPOUNDS |
| FR2587332A1 (en) * | 1985-09-19 | 1987-03-20 | Rhone Poulenc Spec Chim | METHOD FOR SELECTIVE CHLORINATION OF PHENOLIC COMPOUNDS |
| JPS63238025A (en) * | 1987-03-05 | 1988-10-04 | ローヌ−.プーラン・シミ | Chlorination of phenol compound |
| CN1035324C (en) * | 1995-02-16 | 1997-07-02 | 建湖县有机化工厂 | Process for production of 2,6-dichlorophenol by using O-chlorophenol |
| US6635787B2 (en) | 2001-12-20 | 2003-10-21 | Sumitomo Chemical Company, Limited | Production method of a 2,6-dichlorophenol compound |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5630332B2 (en) | 1981-07-14 |
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