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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226855Generated: November 1, 2026

Benzyl mercaptan → HCID 18963786, compound

https://huagongshe.com/reaction/2226855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
Reactant3-Chloro-5-methoxybenzo[b]thiophene-2-carboxamideHCID 10681595—
Reactant3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 18963786HCID 1896378663%

Reaction Conditions

Temperature50 °C

Reaction Steps

Benzylmercaptan (134 μL, 1.14 mmol) is added to a suspension of 3-chloro-5-methoxybenzo[b]thiophene-2-carboxamide (250 mg, 1.03 mmol) in 2 mL of DMF. Diazabicycloundecene (DBU) (170 μL, 1.14 mmol) is added and the mixture is warmed to 50° C. After 1 hour, the reaction mixture is allowed to cool and then is diluted with ethyl acetate and washed with 1N NaOH, 1N HCl, water, and brine. The organic layer is dried over MgSO4. Filtration followed by concentration in vacuo and recrystallization from ethyl acetate: hexane gives 5-methoxy-3-[(phenylmethyl)thio]benzo[b]thiophene-2-carboxamide in 63% yield; mp=151°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350748
Source datasetuspto-grants-1994_09
ORD IDord-2a6db4ebf37f46ea9f3f692c283d5968
Source noteuspto-grants-1994_09