GB303467A - Process for the manufacture of substituted indoles - Google Patents
Process for the manufacture of substituted indolesInfo
- Publication number
- GB303467A GB303467A GB2622327A GB2622327A GB303467A GB 303467 A GB303467 A GB 303467A GB 2622327 A GB2622327 A GB 2622327A GB 2622327 A GB2622327 A GB 2622327A GB 303467 A GB303467 A GB 303467A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sodamide
- toluidine
- sodium
- diethylaniline
- diluent
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
Abstract
303,467. Carpmael, A., (I. G. Farbenindustrie Akt.-Ges.). Oct. 4, 1927. Substituted indoles are prepared by heating a monoacylamino compound of the aromatic series having a methyl group in the ortho position with sodamide in the presence of a diluent. That part of the sodamide which is utilized in forming the sodium salt of the acylamino compound may be replaced by metallic sodium. The diluent may be distilled off during the process. According to examples aceto-o-toluidine is heated with sodamide and metallic sodium in the presence of a solvent such as. naphthalene, dimethylaniline, diethylaniline or other tertiary aromatic amine whereby alpha-methyl indole is produced. In a second example, sodium aceto-o-toluidine and sodamide are heated in the presence of a solvent and in a further example 2 : 5-dimethylindole is obtained by heating 2-acetylamino-1 : 5-dimethylbenzene with sodamide and diethylaniline. In a similar manner 2 : 7-dimethylindol is obtained from .acetylated vic m-xylidine and a-phenylindole from benzoyl-o-toluidine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2622327A GB303467A (en) | 1927-10-04 | 1927-10-04 | Process for the manufacture of substituted indoles |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2622327A GB303467A (en) | 1927-10-04 | 1927-10-04 | Process for the manufacture of substituted indoles |
Publications (1)
Publication Number | Publication Date |
---|---|
GB303467A true GB303467A (en) | 1929-01-04 |
Family
ID=10240258
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2622327A Expired GB303467A (en) | 1927-10-04 | 1927-10-04 | Process for the manufacture of substituted indoles |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB303467A (en) |
-
1927
- 1927-10-04 GB GB2622327A patent/GB303467A/en not_active Expired
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