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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846622Generated: October 30, 2026

Acetone → α-Cyclopropyl-4-(methylthio)benzenemethanol

https://huagongshe.com/reaction/846622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantCyclopropyl[4-(methylsulfanyl)phenyl]methanoneHCID 13533274—
SolventChloroformHCID 6212—
Productα-Cyclopropyl-4-(methylthio)benzenemethanolHCID 1498832974.2%

Reaction Steps

To 200 ml of methanol solution containing 24 g of cyclopropyl (4-methylthiophenyl)ketone was added slowly 9.4 g of sodium borohydride under an ice-cooled condition, the reaction mixture was stirred for 2 hours. Then an adequate amount of acetone was added to the reaction mixture and concentrated under a reduced pressure. To the residue thus obtained was added chloroform, and the chloroform solution was washed with water, dried with anhydrous sodium sulfate, and the solvent was removed by evaporation to yield 18 g of 1-(cyclopropyl, hydroxylmethyl)-4-methylthiobenzene as in the form of colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137889
Source datasetuspto-grants-1992_08
ORD IDord-5103d4df205549d684f7607cc47b20fd
Source noteuspto-grants-1992_08