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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655207Generated: October 31, 2026

Methanol → 3,4-Dichloro-2-(hydroxymethyl)pyridine

https://huagongshe.com/reaction/1655207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3,4-Dichloro-2-methylpyridineHCID 21922890—
SolventDichloromethaneHCID 6344—
Product3,4-Dichloro-2-(hydroxymethyl)pyridineHCID 22117301—

Reaction Steps

m-Chloroperbenzoic acid (32.63 g) in dichloromethane (400 ml) was added dropwise to a solution of 3,4 -dichloro-2 -picoline (25.53 g)in dichloromethane (100 ml) maintaining the temperature at 20°-25°. After standing for 16 hours at room temperature the solution was washed with 1 N NAOH, dried (K2CO3 ) and filtered to give a pale yellow solution. Trifluoroacetic anhydride (30 ml) was added dropwise to this solution maintaining the temperature at 15°-20°. After standing for 2 days at room temperature, methanol (100 ml) was added and the solution evaporated under reduced presure. The residue was treated with aqueous sodium carbonate and extracted into dichloromethane. After drying (K2CO3 ) and removal of solvent, the residue was recrystallised from pet. ether (60/80 ) to give 3,4 -dichloro-2 -hydroxymethylpyridine, 15.76 g, m.p. 66°-8°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250527
Source datasetuspto-grants-1993_10
ORD IDord-080221254b7f41feb105af8a698e71e2
Source noteuspto-grants-1993_10