Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165378Generated: October 30, 2026

Dichloromethane → 4-Cyanophenylethyl cyclopropyl carbinol

https://huagongshe.com/reaction/2165378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBorohydrideHCID 28123—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13316970HCID 13316970—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-Cyanophenylethyl cyclopropyl carbinolHCID 1331697199.3%

Reaction Steps

To a solution of 30.9 g of 4-cyanophenylethyl cyclopropyl ketone in 90 ml of absolute ethanol was added 1.48 g of soldium borohydride, and the mixture was stirred at room temperature for three hours. The product isolated from the reaction still contained unreacted starting material, so the material was redissolved in 90 ml of ethanol and treated with 0.7 g additional sodium borohydride for three hours. The product obtained by evaporation of the solvent, trituration of the residue with methylene dichloride and water, and isolation of the product from the organic phase, gave 31.0 g of 4-cyanophenylethyl cyclopropyl carbinol as an oil which crystallized to a colorless solid, m.p. 70°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939267
Source datasetuspto-grants-1990_07
ORD IDord-edfbe1af0286485e98f31e326409ee19
Source noteuspto-grants-1990_07