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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679894Generated: October 31, 2026

Sodium borohydride → (2-Chloro-6-methylphenyl)methanol

https://huagongshe.com/reaction/1679894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Chloro-6-methylbenzaldehydeHCID 12467050—
SolventMethanolHCID 887—
Product(2-Chloro-6-methylphenyl)methanolHCID 2057902385.6%

Reaction Steps

A solution of 24 g of 2-chloro-6-methylbenzaldehyde [L. G. Humber, J. Med. Chem., 7, 826 (1964)] in 200 ml of methanol is cooled in an ice bath while 6.0 g of sodium borohydride is added in portions. After stirring overnight at room temperature, the mixture is concentrated to dryness and the residue is partitioned between water and ether. The organic layer is washed with dilute hydrochloric acid, dried, and concentrated to yield the crude product. Recrystallization from benzene/hexane gives 20.8 g of 2-chloro-6-methylbenzyl alcohol, mp 83°-86° C. in two crops.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04271164
Source datasetuspto-grants-1981_06
ORD IDord-a87ba4c33ad2409c91c402c909378b6b
Source noteuspto-grants-1981_06