Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087137Generated: October 31, 2026

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

https://huagongshe.com/reaction/1087137

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 numberUS05034395
Source datasetuspto-grants-1991_07
ORD IDord-5ffa4fc8c9e247ef9ec4b4a7180722be
Source noteuspto-grants-1991_07