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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323569Generated: October 30, 2026

Sodium borohydride → 2-(4-Fluoro-3-methyl-phenyl)-4,6-dimethylbenzyl alcohol

https://huagongshe.com/reaction/323569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-(4-Fluoro-3-methyl-phenyl)-4,6-dimethylbenzaldehydeHCID 13316979—
SolventEthanolHCID 702—
Product2-(4-Fluoro-3-methyl-phenyl)-4,6-dimethylbenzyl alcoholHCID 1331698098.9%

Reaction Steps

2.90 grams (12 mmol) of 2-(4-fluoro-3-methyl-phenyl)-4,6-dimethylbenzaldehyde (prepared according to Stokker, Jour. Med. Chem. Vol. 29 p.170, 1986) was reduced with 0.454 grams (12 mmol) of sodium borohydride in ethanol (20 mL) at 0 ° C. The reaction was stirred 1 hr, quenched with aqueous ammonium chloride and the mixture extracted with ether. The organic portion was dried (MgSO4) and concentrated to give 2.90 grams of 2-(4-fluoro-3-methyl-phenyl)-4,6-dimethylbenzyl alcohol as an oil which solidified on standing. The crude solid was treated with 1.31 mL of thionyl chloride and heated on a steam bath for 1 hour. After cooling to room temperature, the crude mixture was taken up in water and extracted with ether. The ether was washed with water and dried (MgSO4), and concentrated to give an oily residue which was purified by silica gel chromatography (25% methylene chloride/75% hexane) to give 2-(4-fluoro-3-methyl-phenyl)-4,6-dimethylbenzyl chloride as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214810B1
Source datasetuspto-grants-2001_04
ORD IDord-a9995bf33c194be0b7c0d5906660396a
Source noteuspto-grants-2001_04