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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068471Generated: November 2, 2026

Acetic Anhydride → 2-Acetoxymethyl-6-benzyloxypyridine

https://huagongshe.com/reaction/1068471

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 numberUS06248756B1
Source datasetuspto-grants-2001_06
ORD IDord-131434c42ae64d43a81c974a65a891b0
Source noteuspto-grants-2001_06