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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443287Generated: October 30, 2026

Acetic Anhydride → 2-Acetoxymethyl-6-benzyloxypyridine

https://huagongshe.com/reaction/443287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant6-Benzyloxy-2-picoline 1-oxideHCID 19744434—
Product2-Acetoxymethyl-6-benzyloxypyridineHCID 21193437—

Reaction Steps

A mixture of 2-benzyloxy-6-methylpyridine N-oxide (3.4 g, 15.9 mmol) and acetic anhydride (125 mL) was heated under reflux for 1 h. The resulting solution was concentrated under vacuum, and the residue was partitioned between aqueous sodium bicarbonate and dichloromethane. The organic extract was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with 10-20% ethyl acetate in hexane gradient. Collection and concentration of appropriate fractions provided 2-acetoxymethyl-6-benzyloxypyridine as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891889
Source datasetuspto-grants-1999_04
ORD IDord-8a922d72e332412f96736906d12d7721
Source noteuspto-grants-1999_04