HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-(5-benzamido-2-chlorophenyl)-2-amino-4-methoxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-(5-benzamido-2-chlorophenyl)-4-methoxy-2-nitrobenzamide | HCID 22238139 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(5-benzamido-2-chlorophenyl)-2-amino-4-methoxybenzamide | HCID 9908705 | 46% |
Reaction Steps
Iron powder (2.79 g) was added to a stirred suspension of N-(5-benzamido-2-chlorophenyl)-4-methoxy-2-nitrobenzamide (2.13 g) in a mixture of ethanol (100 ml), water (20 ml) and acetic acid (4 ml). The mixture was stirred and heated to reflux for 6 hours. The mixture was cooled to ambient temperature. Water (50 ml) was added and the resultant mixture was basified by the addition of sodium carbonate. The mixture was filtered and the filtrate was evaporated. The residue was triturated under water. The resultant solid was isolated and dried under vacuum at 40° C. There was thus obtained the title compound (0.911 g);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06465455B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-496ac22ec8004cff908f5ec448e0236a |
| Source note | uspto-grants-2002_10 |