NL7703353A - Para:amino-azobenzene prodn. - by reacting excess aniline with an alkali nitrite in hydrochloric acid medium contg. dissolved oxygen - Google Patents
Para:amino-azobenzene prodn. - by reacting excess aniline with an alkali nitrite in hydrochloric acid medium contg. dissolved oxygenInfo
- Publication number
- NL7703353A NL7703353A NL7703353A NL7703353A NL7703353A NL 7703353 A NL7703353 A NL 7703353A NL 7703353 A NL7703353 A NL 7703353A NL 7703353 A NL7703353 A NL 7703353A NL 7703353 A NL7703353 A NL 7703353A
- Authority
- NL
- Netherlands
- Prior art keywords
- contg
- prodn
- azobenzene
- para
- amino
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B37/00—Azo dyes prepared by coupling the diazotised amine with itself
Abstract
Aminoazobenzene (I) is made by reacting excess aniline at 100 degrees C with an alkali nitrite in HCl medium contg. >=30 ppm dissolved elementary O2, and allowing the diazoaminobenzene cpd. formed to isomerise in the same soln. The reaction mixt. is then neutralised with caustic alkali and the aq. phase is sepd. from the organic phase contg. the (I) dissolved in aniline. The required dissolved O2 level can be achieved e.g. by carrying out the reaction under air at a pressure of >=2 atmos. or under a protective gas contg. >=40 vol. % O2, or by bubbling a protective gas contg. >=40 vol. % O2 through the reaction medium. The presence of O2 in the reaction medium reduces the formation of by-prods. such as o-aminobenzene, diphenylamine, 2-, 3- and 4-aminobiphenyl and 'diazo tars', and gives (I) of high purity. (I) is suitable for hydrogenation into p-phenylenediamine, which is a useful raw material in the mfr. of aromatic fibre-forming polyamides.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL7703353A NL7703353A (en) | 1977-03-29 | 1977-03-29 | Para:amino-azobenzene prodn. - by reacting excess aniline with an alkali nitrite in hydrochloric acid medium contg. dissolved oxygen |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL7703353A NL7703353A (en) | 1977-03-29 | 1977-03-29 | Para:amino-azobenzene prodn. - by reacting excess aniline with an alkali nitrite in hydrochloric acid medium contg. dissolved oxygen |
Publications (1)
Publication Number | Publication Date |
---|---|
NL7703353A true NL7703353A (en) | 1978-10-03 |
Family
ID=19828260
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL7703353A NL7703353A (en) | 1977-03-29 | 1977-03-29 | Para:amino-azobenzene prodn. - by reacting excess aniline with an alkali nitrite in hydrochloric acid medium contg. dissolved oxygen |
Country Status (1)
Country | Link |
---|---|
NL (1) | NL7703353A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4376730A (en) | 1981-03-13 | 1983-03-15 | Akzo N.V. | Preparation of p-aminoazo-benzene from aniline |
EP0035815B1 (en) * | 1980-03-12 | 1983-06-08 | Akzo N.V. | Process for the preparation of p-aminoazobenzene from aniline |
-
1977
- 1977-03-29 NL NL7703353A patent/NL7703353A/en not_active Application Discontinuation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0035815B1 (en) * | 1980-03-12 | 1983-06-08 | Akzo N.V. | Process for the preparation of p-aminoazobenzene from aniline |
US4376730A (en) | 1981-03-13 | 1983-03-15 | Akzo N.V. | Preparation of p-aminoazo-benzene from aniline |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
BV | The patent application has lapsed |