HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 4-Anilino-3-nitro-5-phenylsulphamyl-benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 4-Chloro-5-chlorosulfonyl-3-nitrobenzoic acid | HCID 89892 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Anilino-3-nitro-5-phenylsulphamyl-benzoic acid | HCID 21506088 | — |
Reaction Steps
To a solution of 4-chloro-3-nitro-5-chlorosulphonyl-benzoic acid (6 g) in ethyl acetate (50 ml), aniline (7.5 g) was added, while stirring. The reaction mixture was stirred for a further 8 hours and filtered. The filtrate was evaporated, and the residue was dissolved in a mixture of aqueous sodium hydrogen carbonate and diethyl ether. The aqueous layer was separated, and the 4-anilino-3-nitro-5-phenylsulphamyl-benzoic acid was precipitated by addition of 4N hydrochloric acid. After recrystallization from aqueous ethanol (25% ethanol in water), the melting point was 249°-250°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03971819 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-7f0fb79a6d864651988750e622130632 |
| Source note | uspto-grants-1976_07 |