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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614460Generated: October 30, 2026

Water → 3-Benzyl-4-fluorobenzyl alcohol

https://huagongshe.com/reaction/1614460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Benzyl-4-fluorobenzaldehydeHCID 13854280—
SolventMethanolHCID 887—
Product3-Benzyl-4-fluorobenzyl alcoholHCID 1385428179.3%

Reaction Steps

A solution of 3-benzyl-4-fluorobenzaldehyde (5 g) in methanol (75 cm3) was cooled to 0° C. Sodium borohydride (1.34 g) was added in portions, and the mixture stirred for 1 hour. The reaction mixture was then poured cautiously into a mixture of water and diethyl ether, and the organic layer was separated, washed with water and brine, and dried over anhydrous magnesium sulphate. Evaporation of the solvents under reduced pressure gave a pale yellow oil which was purified by distillation in a kugelrohr apparatus to give 3-benzyl-4-fluorobenzyl alcohol (4.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05196610
Source datasetuspto-grants-1993_03
ORD IDord-17061e3314e14e26a0cbd12ac815ba2d
Source noteuspto-grants-1993_03