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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381172Generated: November 2, 2026

Triethylamine → 1-Acetyl-3-(benzyloxy)-2-methylpyridin-4(1H)-one

https://huagongshe.com/reaction/1381172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcetyl bromideHCID 10482—
Reactant2-Methyl-3-(phenylmethoxy)-4(3H)-pyridinoneHCID 69343794—
SolventAcetoneHCID 180—
Product1-Acetyl-3-(benzyloxy)-2-methylpyridin-4(1H)-oneHCID 1868877664.8%

Reaction Steps

1 3-Benzyloxy-2-methylpyrid-4-one (4 g) is dissolved in dry acetone (100 ml). Acetylbromide (3 g) and triethylamine (2.7 g) are added and the resulting mixture is mechanically stirred overnight. The mixture is then filtered and the filtrate is rotary evaporated to dryness. The residue is dissolved in methylene chloride and washed with dilute hydrochloric acid (pH 3.0), then twice with water, and is dried over Na2SO4 and rotary evaporated to yield a solid residue. Recrystallisation of this residue from an ethylacetate/hexane mixture gives 1-acetyl-3-benzyloxy-2-methylpyrid-4-one as an oil (3.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585780
Source datasetuspto-grants-1986_04
ORD IDord-71ac59d3527e486c810f7ddf29d012d0
Source noteuspto-grants-1986_04