GB816855A - Improved processes of manufacture of 4-bromo-4-nitrocarbanilide - Google Patents
Improved processes of manufacture of 4-bromo-4-nitrocarbanilideInfo
- Publication number
- GB816855A GB816855A GB28256A GB28256A GB816855A GB 816855 A GB816855 A GB 816855A GB 28256 A GB28256 A GB 28256A GB 28256 A GB28256 A GB 28256A GB 816855 A GB816855 A GB 816855A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nitrocarbanilide
- bromo
- manufacture
- improved processes
- bromination
- 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
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 6
- 238000005893 bromination reaction Methods 0.000 abstract 2
- 239000003701 inert diluent Substances 0.000 abstract 2
- 239000012442 inert solvent Substances 0.000 abstract 2
- 230000003993 interaction Effects 0.000 abstract 2
- PFQUUCXMPUNRLA-UHFFFAOYSA-N (4-bromophenyl)urea Chemical compound NC(=O)NC1=CC=C(Br)C=C1 PFQUUCXMPUNRLA-UHFFFAOYSA-N 0.000 abstract 1
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-Dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 abstract 1
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-Nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C273/18—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas
- C07C273/1854—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas by reactions not involving the formation of the N-C(O)-N- moiety
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
4-Bromo-41-nitrocarbanilide is prepared either by bromination of 4-nitrocarbanilide or by interaction of p-bromophenylurea and p-nitroaniline. The bromination is advantageously carried out in the presence of an inert diluent or solvent, e.g. acetic acid, either at ordinary temperatures, e.g. about 15 DEG to 25 DEG C., or at elevated temperatures, e.g. about 90 DEG to 95 DEG C. The interaction is also preferably carried out in an inert diluent or solvent, e.g. o-dichlorobenzene or acetic acid. Examples are given. Specification 816,856, [Group VI], is referred to.
Publications (1)
Publication Number | Publication Date |
---|---|
GB816855A true GB816855A (en) | 1959-07-22 |
Family
ID=1593309
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB28256A Expired GB816855A (en) | 1956-01-04 | Improved processes of manufacture of 4-bromo-4-nitrocarbanilide |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB816855A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0531689A1 (en) * | 1991-08-16 | 1993-03-17 | Chemie Linz GmbH | Process for the preparation of pure N,N'-asymmetrically substituted phenylureas |
-
1956
- 1956-01-04 GB GB28256A patent/GB816855A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0531689A1 (en) * | 1991-08-16 | 1993-03-17 | Chemie Linz GmbH | Process for the preparation of pure N,N'-asymmetrically substituted phenylureas |
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