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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583464Generated: October 31, 2026

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

https://huagongshe.com/reaction/1583464

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 0.1N 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 numberUS04551546
Source datasetuspto-grants-1985_11
ORD IDord-7a0341657020433ea1fff5fd0d14e82c
Source noteuspto-grants-1985_11