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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464299Generated: October 25, 2026

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

https://huagongshe.com/reaction/1464299

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 numberUS05304556
Source datasetuspto-grants-1994_04
ORD IDord-417f44e2e8774e5bb426b3d89b2514ab
Source noteuspto-grants-1994_04