Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359793Generated: October 29, 2026

Water → 4-Cyanophenylethyl cyclopropyl carbinol

https://huagongshe.com/reaction/359793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13316970HCID 13316970—
SolventEthanolHCID 702—
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 sodium 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 numberUS05002960
Source datasetuspto-grants-1991_03
ORD IDord-a0dd0ebe654a4a2690cc0f6b32574b4e
Source noteuspto-grants-1991_03