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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701213Generated: November 1, 2026

Water → N-(7-Hydroxy-4,5,6,7-tetrahydro-1-benzothiophen-4-yl)urea

https://huagongshe.com/reaction/1701213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulbenoxHCID 65473—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductN-(7-Hydroxy-4,5,6,7-tetrahydro-1-benzothiophen-4-yl)ureaHCID 20348930—

Reaction Steps

In 2.5 liters of ethanol, 34.85 grams of (-)-4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-ylurea is stirred and 9.8 grams of NaBH4 is added. The mixture is stirred overnight at room temperature, 1400 ml. of water is added, and after stirring for 0.5 hour the ethanol is evaporated in vacuo. The mixture is cooled and 25-30 ml. of acetic acid is added until no more foaming occurs. The mixture is stirred for 0.75 hour, filtered to collect the first crop and this solid is washed with water and air dried. This solid is recrystallized from acetone and then from acetone/methanol to give 6.75 g. of isomer B of the title compound, m.p. 211°-213° C. (dec.), [α]D25.5 =-23.23° (c, 3.11 in methanol). This material contains 92% isomer B and 8% isomer A when assayed by high pressure liquid chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04191830
Source datasetuspto-grants-1980_03
ORD IDord-2a9d414efec94b42bc2ab2b66d1d0fe1
Source noteuspto-grants-1980_03