Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443434Generated: October 30, 2026

m,alpha-Dichlorotoluene → 5-(m-Chlorobenzyloxy)-2-pyridinemethanol

https://huagongshe.com/reaction/443434

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm,alpha-DichlorotolueneHCID 12103—
ReactantSodiumHCID 5360545—
Reactant6-(Hydroxymethyl)pyridin-3-ol hydrochlorideHCID 18758423—
SolventMethanolHCID 887—
Product5-(m-Chlorobenzyloxy)-2-pyridinemethanolHCID 23467167—

Reaction Steps

The solution of 16.2 g of 5-hydroxy-2-pyridinemethanol hydrochloride in 150 ml of methaol is added to a solution of 4.6 g of sodium in 250 ml of methanol, while stirring, over a period of 25 minutes. The solution is stirred for one hour and then a solution of 19.3 g of m-chlorobenzyl chloride in 50 ml of methanol is added. Then the mixture is refluxed for 19 hours, cooled, filtered and the filtrate evaporated to a residue. The residue is suspended in 100 ml of water, made basic with 20% aqueous sodium hydroxide solution and then extracted with chloroform. The chloroform extract is separated, dried over sodium sulfate, filtered and the filtrate evaporated, to yield 5-(m-chlorobenzyloxy)-2-pyridinemethanol melting at 78°-80°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04260620
Source datasetuspto-grants-1981_04
ORD IDord-664c549644df454194d948c9d7af61de
Source noteuspto-grants-1981_04