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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934712Generated: October 31, 2026

4-Cyanobenzaldehyde → p-Cyanobenzyl alcohol

https://huagongshe.com/reaction/1934712

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Productp-Cyanobenzyl alcoholHCID 16054993.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 4-cyanobenzaldehyde (5.00 g) in ethanol (50 mL) and tetrahydrofuran (20 mL) was added sodium borohydride (2.16 g) under ice-water cooling, and the mixture was stirred for an hour at 0° C. After evaporation of the solvent, the residue was partitioned between ethyl acetate and water. The separated organic layer was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo to give 4-cyanobenzyl alcohol (4.76 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384080B1
Source datasetuspto-grants-2002_05
ORD IDord-f9ca8c348cb74a35afd516e14b5e4c60
Source noteuspto-grants-2002_05