HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Anilino-3-nitro-5-sulphamyl-benzoic acid → 3-Amino-5-sulphamyl-4-(m-trifluoromethylanilino)-benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Anilino-3-nitro-5-sulphamyl-benzoic acid | HCID 21506071 | — |
| Reactant | 3-Nitro-5-sulphamyl-4-(m-trifluoromethylanilino)-benzoic acid | HCID 21506111 | — |
| Product | 3-Amino-5-sulphamyl-4-(m-trifluoromethylanilino)-benzoic acid | HCID 21506057 | — |
Reaction Steps
By substituting 3-nitro-5-sulphamyl-4-(m-trifluoromethylanilino)-benzoic acid for the 4-anilino-3-nitro-5-sulphamyl-benzoic acid of Example 9 B, the above compound was obtained with a melting point of 273°-274° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03985777 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-c534dedbb67f40ca886408e7846a3029 |
| Source note | uspto-grants-1976_10 |