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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl mercaptanHCID 7509—
ReactantSodium hydrideHCID 24758—
ReactantMethanone, (5-bromo-2-thienyl)(4-methoxyphenyl)-HCID 298606—
SolventDimethylformamideHCID 6228—
Product(4-Methoxyphenyl)[5-[(phenylmethyl)thio]-2-thienyl]methanoneHCID 13364599—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04486444
Source datasetuspto-grants-1984_12
ORD IDord-f1d6fc5116004de9b68c5f6380bbb4e5
Source noteuspto-grants-1984_12