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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296512Generated: October 30, 2026

Sodium borohydride → 3-Methyl-2,4,5,6-tetrafluorobenzyl alcohol

https://huagongshe.com/reaction/2296512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Methyl-2,4,5,6-tetrafluorobenzaldehydeHCID 13075318—
SolventMethanolHCID 887—
Product3-Methyl-2,4,5,6-tetrafluorobenzyl alcoholHCID 1307531979.2%

Reaction Steps

Sodium borohydride (0.3 g) was added in small portions to a solution of 3-methyl-2,4,5,6-tetrafluorobenzaldehyde (1.5 g) in methyl alcohol (15 ml) at the ambient temperature, after which the mixture was heated at the reflux temperature for 30 minutes. The methyl alcohol was removed by evaporation under reduced pressure and the residue partitioned between dilute hydrochloric acid (20 ml of a 0.1 N solution) and ether (20 ml). The ethereal phase was separated, washed with saturated sodium bicarbonate solution and with water and then dried over anhydrous magnesium sulphate. After evaporation of the ether under reduced pressure the product was distilled in a Kugelrohr apparatus to yield 3-methyl-2,4,5,6-tetrafluorobenzyl alcohol (1.2 g)--approximate b.p. 100° C./14 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04429153
Source datasetuspto-grants-1984_01
ORD IDord-877896ef25a740b59fe60bd58c99288b
Source noteuspto-grants-1984_01