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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614455Generated: October 26, 2026

Sodium borohydride → 3-Benzylbenzyl alcohol

https://huagongshe.com/reaction/1614455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-BenzylbenzaldehydeHCID 13102743—
ReactantDiethylether waterHCID 21584184—
SolventMethanolHCID 887—
Product3-Benzylbenzyl alcoholHCID 59761393.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Benzylbenzaldehyde (5.5 g) was dissolved in methanol (75 cm3) and cooled to 0° C. Sodium borohydride (1.29 g) was added gradually in small portions, and stirring was continued for one hour. The reaction mixture was cautiously poured into a water/diethyl ether mixture, and the resulting ethereal solution was washed with water and brine, and dried over anhydrous magnesium sulphate. Evaporation of the solvents under reduced pressure gave 3-benzylbenzyl alcohol as a pale yellow oil (5.2 g). The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05196610
Source datasetuspto-grants-1993_03
ORD IDord-c1e47ff332e743689be6b776dd985ec0
Source noteuspto-grants-1993_03