JPS57169447A - Preparation of 2,4-dichloro- or 2,6-dichloroaniline - Google Patents
Preparation of 2,4-dichloro- or 2,6-dichloroanilineInfo
- Publication number
- JPS57169447A JPS57169447A JP56054088A JP5408881A JPS57169447A JP S57169447 A JPS57169447 A JP S57169447A JP 56054088 A JP56054088 A JP 56054088A JP 5408881 A JP5408881 A JP 5408881A JP S57169447 A JPS57169447 A JP S57169447A
- Authority
- JP
- Japan
- Prior art keywords
- dichloroaniline
- dichloro
- acid
- bromonitrobenzene
- dichlorobenzene
- 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
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
PURPOSE: To obtain the titled compound useful as a raw material for agricultural chemicals, medicines, dyes, etc. easily, by reacting a 1-bromo-3,5-dichlorobenzene with a mixed acid at a specific temperature, and reacting the resultant reaction product with H2 in the presence of a catalyst at a specific temperature under pressure.
CONSTITUTION: 1-Bromo-3,5-dichlorobenzene is reacted with a mixed acid, e.g. nitric acid with sulfuric acid, at 0W150°C to give 2,4-dichloro-6-bromonitrobenzene or 2,6-dichloro-4-bromonitrobenzene. In case a solvent is used, acetic acid, sulfuric acid or carbon tetrachloride is used. The resultant bromodichloronitrobenzene is then reacted with H2 in the presence of a catalyst, e.g. Pd, Pt or Ni, at 50W200°C and a pressure of 2W100kg/cm2.G to afford 2,4-dichloroaniline or 2,6-dichloroaniline.
EFFECT: The aimed substance is obtained in high yield well in one stage with the inhibited formation of by-products.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56054088A JPS57169447A (en) | 1981-04-10 | 1981-04-10 | Preparation of 2,4-dichloro- or 2,6-dichloroaniline |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56054088A JPS57169447A (en) | 1981-04-10 | 1981-04-10 | Preparation of 2,4-dichloro- or 2,6-dichloroaniline |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57169447A true JPS57169447A (en) | 1982-10-19 |
JPS6356216B2 JPS6356216B2 (en) | 1988-11-07 |
Family
ID=12960859
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56054088A Granted JPS57169447A (en) | 1981-04-10 | 1981-04-10 | Preparation of 2,4-dichloro- or 2,6-dichloroaniline |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57169447A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60130553A (en) * | 1983-12-19 | 1985-07-12 | Central Glass Co Ltd | Preparation of 4-chloro-2-trifluoromethylaniline |
JP2011524402A (en) * | 2008-06-16 | 2011-09-01 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Method for producing an intermediate for the synthesis of dabigatran |
-
1981
- 1981-04-10 JP JP56054088A patent/JPS57169447A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60130553A (en) * | 1983-12-19 | 1985-07-12 | Central Glass Co Ltd | Preparation of 4-chloro-2-trifluoromethylaniline |
JP2011524402A (en) * | 2008-06-16 | 2011-09-01 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Method for producing an intermediate for the synthesis of dabigatran |
Also Published As
Publication number | Publication date |
---|---|
JPS6356216B2 (en) | 1988-11-07 |
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