HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 2-Oxo-N-phenyl-2,3-dihydro-1-benzothiophene-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Ethyl 2-oxo-2,3-dihydro-1-benzothiophene-3-carboxylate | HCID 20493680 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-Oxo-N-phenyl-2,3-dihydro-1-benzothiophene-3-carboxamide | HCID 12799385 | — |
Reaction Steps
470 mg (2.11 mmols) of ethyl 2-oxo-2,3-dihydro-3-benzo[b]thiophene-carboxylate and 206 mg (2.22 mmols) of aniline in 3 ml of xylene are boiled under reflux for 5 hours. After cooling, the product is precipitated by adding hexane (3 ml). After further dilution with 5 ml of ether and stirring, crystalline N-phenyl-2-oxo-2,3-dihydro-3-benzo[b]thiophene-carboxamide with a melting point of 140°-142° is obtained and filtered off.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04260779 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-d81d7d2afabd41c4933fad7e7bf140d6 |
| Source note | uspto-grants-1981_04 |