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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728801Generated: October 31, 2026

Acetic Anhydride → N-(4-Pyridinylmethyl)acetamide

https://huagongshe.com/reaction/1728801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-PyridinemethanamineHCID 77317—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductN-(4-Pyridinylmethyl)acetamideHCID 289830—

Reaction Steps

The title compound is prepared by the procedure of Example 12 using 25 g of 4-(aminomethyl)pyridine, 25.1 ml of acetic anhydride, 2.26 g of 4-dimethylaminopyridine, 80 ml of pyridine and stirring at room temperature for 68 hours. The residue is purified by column chromatography (silica gel:20% methyl alcohol/ethyl acetate) to give 3.82 g of desired product as orange crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05328921
Source datasetuspto-grants-1994_07
ORD IDord-a54e7c903e254a6189f4a7b3fdb5a542
Source noteuspto-grants-1994_07