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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194036Generated: October 30, 2026

Water → 3-Benzyl-4-fluorobenzyl alcohol

https://huagongshe.com/reaction/1194036

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 mixure 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 numberUS04812483
Source datasetuspto-grants-1989_03
ORD IDord-da2a8514d4c1432db08341fe746378a4
Source noteuspto-grants-1989_03