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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380078Generated: November 1, 2026

Cyclohexyl bromide → 3-Methyl-1-benzothiophene-7-ol

https://huagongshe.com/reaction/1380078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl bromideHCID 7960—
ReactantTetrahydrofuranHCID 8028—
ReactantMagnesiumHCID 5462224—
Reactant7-Chloro-3-methyl-1-benzothiopheneHCID 20242118—
Product3-Methyl-1-benzothiophene-7-olHCID 15324807—

Reaction Steps

Cyclohexyl bromide (32.6 g.) and 7-chloro-3-methylbenzo[b]thiophene (18.3 g.) in THF (400 ml) is added to a suspension of magnesium turnings (7.3 g.) in THF. The mixture is stirred for two hours and heated on a steam bath for two hours. The reaction is cooled and oxygen is bubbled in slowly for two hours. The mixture is stirred for 18 hours at room temperature and extracted with chloroform. The organic extract is extracted with 5% sodium hydroxide. The aqueous extract is acidified with concentrated hydrochloric acid and extracted with ethyl ether. The ether extract is dried (MgSO4) and concentrated to a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579865
Source datasetuspto-grants-1986_04
ORD IDord-21ec5330ac1945778ad9edafb0969c2b
Source noteuspto-grants-1986_04