GB514329A - Manufacture of aliphatic ketone-anils - Google Patents
Manufacture of aliphatic ketone-anilsInfo
- Publication number
- GB514329A GB514329A GB13147/38A GB1314738A GB514329A GB 514329 A GB514329 A GB 514329A GB 13147/38 A GB13147/38 A GB 13147/38A GB 1314738 A GB1314738 A GB 1314738A GB 514329 A GB514329 A GB 514329A
- Authority
- GB
- United Kingdom
- Prior art keywords
- anil
- ketone
- aliphatic
- anils
- pinacoline
- 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
- C07C249/00—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C249/02—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of compounds containing imino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
514,329. Aliphatic ketone-anils. I. G. FARBENINDUSTRIE AKT.-GES. May 3, 1938, No. 13147. Convention date, May 27, 1937. [Class 2 (iii)] Aliphatic ketone-anils are made by condensing an aliphatic ketone with aniline or a homologue thereof in the absence of a dehydrating agent, by continuously distilling off from the mixture water produced by the reaction. The distillation may be performed in the apparatus of H. Meyer (Annalen vol. 433, p. 331). In the case of water soluble ketones, benzene or toluene may be added to the mixture. Examples are methylisobutyl ketone-anil; n-propylmethyl ketone-anil; ipropylmethyl ketone-anil ; n-butylmethyl ketone-anil ; pinacoline-anil ; di-n-propylketone-anil ; di-iso-propylketone-anil ;methylnonyl ketone-anil; ethylmethyl ketone-anil; acetone-anil ; pinacoline-o, m or p-tolil. Acetone-anil is stated to combine with 1 molecule of aniline to produce a diphenamine compound. Reduced, the aliphatic ketoneanils yield amines which are useful dyestuff intermediates.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1937I0058106 DE693988C (en) | 1937-05-28 | 1937-05-28 | Process for the preparation of aliphatic ketoanils |
Publications (1)
Publication Number | Publication Date |
---|---|
GB514329A true GB514329A (en) | 1939-11-06 |
Family
ID=7194700
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB13147/38A Expired GB514329A (en) | 1937-05-28 | 1938-05-03 | Manufacture of aliphatic ketone-anils |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE693988C (en) |
GB (1) | GB514329A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3014967A (en) * | 1957-01-11 | 1961-12-26 | Monsanto Chemicals | Preparation and hydrogenation of schiff's bases |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH647501A5 (en) * | 1980-04-30 | 1985-01-31 | Lonza Werke Gmbh | 2,6-DICHLORO-5-HYDROXY-ANILE AND PROCESS FOR PRODUCTION THEREOF. |
-
1937
- 1937-05-28 DE DE1937I0058106 patent/DE693988C/en not_active Expired
-
1938
- 1938-05-03 GB GB13147/38A patent/GB514329A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3014967A (en) * | 1957-01-11 | 1961-12-26 | Monsanto Chemicals | Preparation and hydrogenation of schiff's bases |
Also Published As
Publication number | Publication date |
---|---|
DE693988C (en) | 1940-07-23 |
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