GB597809A - Improvements in or relating to derivatives of diphenyl - Google Patents
Improvements in or relating to derivatives of diphenylInfo
- Publication number
- GB597809A GB597809A GB1927/44A GB192744A GB597809A GB 597809 A GB597809 A GB 597809A GB 1927/44 A GB1927/44 A GB 1927/44A GB 192744 A GB192744 A GB 192744A GB 597809 A GB597809 A GB 597809A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino group
- produced
- nitrobiphenyl
- reduction
- treatment
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/38—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reaction of ammonia or amines with sulfonic acids, or with esters, anhydrides, or halides thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/02—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof
- C07C303/04—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups
- C07C303/08—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups by reaction with halogenosulfonic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Amino-diphenyl derivatives of the general formula <FORM:0597809/IV/1> where X is chlorine or -NH2 and A is an amino group or a group convertible into an amino group by hydrolysis or reduction are made by a process which comprises the treatment of a compound of the formula <FORM:0597809/IV/2> where B is a group convertible into an amino group by reduction or hydrolysis with chlorsulphonic acid, treatment of the sulphonyl chloride so formed with ammonia and finally hydrolysis or reduction to form the amino group. To prepare the starting materials: (a) diphenyl is nitrated with a mixture of nitric and sulphuric acids and the required 2-nitrobiphenyl is separated; (b) the 2-nitrobiphenyl prepared as above is reduced with hydrochloric acid and iron filings; (c) the aminobiphenyl produced in (b) is acetylated by treatment with acetic anhydride. In examples, (1) the 2-acetylaminobiphenyl prepared above is treated with chlorsulphonic acid to produce p - (o - acetamidophenyl) benzenesulphonyl chloride; (2) the compound produced in concentrated ammonia; (3) the amination product of example (2) above is hydrolyzed to give p-(o-aminophenylbenzenesulphonamide; (4) 2-nitrobiphenyl produced as above is treated with chlorsulphonic acid; (5) p-(o-nitrophenyl)benzenesulphonyl chloride is aminated with concentrated ammonium hydroxide to p - (o - nitrophenyl) - benzenesulphonamide. (6) the compound produced in example (5) is reduced with tin and hydrochloric acid to form the same compound as was formed in example (3) above.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US597809XA | 1943-04-12 | 1943-04-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB597809A true GB597809A (en) | 1948-02-04 |
Family
ID=22025171
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1927/44A Expired GB597809A (en) | 1943-04-12 | 1944-02-02 | Improvements in or relating to derivatives of diphenyl |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB597809A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104292156A (en) * | 2014-10-15 | 2015-01-21 | 江苏耕耘化学有限公司 | Boscalid homologs and uncoupling synthesis method thereof as well as application of boscalid homologs in preparing medicines for preventing and treating pathogenic bacteria |
-
1944
- 1944-02-02 GB GB1927/44A patent/GB597809A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104292156A (en) * | 2014-10-15 | 2015-01-21 | 江苏耕耘化学有限公司 | Boscalid homologs and uncoupling synthesis method thereof as well as application of boscalid homologs in preparing medicines for preventing and treating pathogenic bacteria |
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