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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259208Generated: October 26, 2026

Cyclohexanone → 2-(1-Hydroxycyclohexyl)-6-methoxybenzothiophene

https://huagongshe.com/reaction/2259208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantAmmonium ChlorideHCID 25517—
Reactant6-Methoxy-1-benzothiopheneHCID 13634237—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(1-Hydroxycyclohexyl)-6-methoxybenzothiopheneHCID 19002769—

Reaction Steps

3.2 g of 6-methoxybenzo[b]thiophene was dissolved in 3 ml of THF and the solution was cooled with ice. 18.6 ml of n-butyllithium (15% hexane solution) was gradually added in a stream of nitrogen and the mixture was stirred. A THF solution of 3.1 ml of cyclohexanone was added and the mixture was stirred at room temperature for 6 hours. 35 ml of saturated aqueous ammonium chloride solution was added to the reaction mixture, the resultant mixture was extracted with ether, and the extract was dried over anhydrous magnesium sulfate. The solvent was distilled off, and the resultant crude product was purified by TLC (developing solvent, chloroform) to obtain 2.8 g of 6-methoxy-2-(1-hydroxycyclohexyl)benzo[b]thiophene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05472962
Source datasetuspto-grants-1995_12
ORD IDord-fad93f897b9a418cb12d655d36b2c33f
Source noteuspto-grants-1995_12