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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609596Generated: October 26, 2026

Acetic Anhydride → 2-acetoxymethyl-5-methoxy-N-(3-pyridylmethyl)benzamide

https://huagongshe.com/reaction/1609596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant2-hydroxymethyl-5-methoxy-N-(3-pyridylmethyl)benzamideHCID 20082005—
SolventDichloromethaneHCID 6344—
Product2-acetoxymethyl-5-methoxy-N-(3-pyridylmethyl)benzamideHCID 20082003100%

Reaction Steps

A solution of 710 mg of 2-hydroxymethyl-5-methoxy-N-(3-pyridylmethyl) benzamide and 317 mg of triethylamine in 10 ml of methylene chloride was chilled at 0° C., mixed with 320 mg of acetic anhydride and stirred at room temperature for 15 hours. The reaction mixture was washed with water and saturated brine in order. The organic layer was dried over anhydrous magnesium sulfate and concentrated in vacuo to give 820 mg of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401756
Source datasetuspto-grants-1995_03
ORD IDord-6561ddaba5174c80b382cf9c5f8839d1
Source noteuspto-grants-1995_03