HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153787Generated: October 31, 2026
Water → (4-Methoxyphenyl)[5-[(phenylmethyl)thio]-2-thienyl]methanone
https://huagongshe.com/reaction/1153787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methanone, (5-bromo-2-thienyl)(4-methoxyphenyl)- | HCID 298606 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (4-Methoxyphenyl)[5-[(phenylmethyl)thio]-2-thienyl]methanone | HCID 13364599 | — |
Reaction Steps
Benzyl mercaptan (1.24 g, 0.01 mol) was added to a stirred mixture of sodium hydride (50% oil dispersion, 0.44 g, 0.11 mol) and degassed DMF (10 mL). The resulting mixture was warmed cautiously until gas evolution ceased. After cooling to 25° C., a solution of 2-bromo-5-(4-methoxybenzoyl)thiophene (2.97 g, 0.01 mol) in DMF (10 mL) was added dropwise. After complete addition, the mixture was heated on the steam bath for 2.5 hours and poured into waTER (200 mL). The aqueous mixture was extracted with ether (2×200 mL) and the extracts were washed with water, saturated NaCl solution and dried (Na2SO4). After evaporation of the solvent, the residue was collected with the aid of hexane and dried, 1.98 g, m.p. 103°-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04486444 |
|---|
| Source dataset | uspto-grants-1984_12 |
|---|
| ORD ID | ord-f1d6fc5116004de9b68c5f6380bbb4e5 |
|---|
| Source note | uspto-grants-1984_12 |
|---|