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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056882Generated: October 29, 2026

Acetic Acid → 3-(benzyloxy)-1-(4-butylphenyl)pyridin-4(1H)-one

https://huagongshe.com/reaction/1056882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-ButylanilineHCID 7694—
Reactant5-(benzyloxy)-4-oxo-4H-pyran-2-carboxylic acidHCID 6480782—
SolventWaterHCID 962—
Product3-(benzyloxy)-1-(4-butylphenyl)pyridin-4(1H)-oneHCID 67419599—

Reaction Steps

A suspension of 4-butyl aniline (0.6 g, 4.1 mmol) and 5˜(benzyloxy)-4-oxo-4H-pyran-2-carboxylic acid (1.0 g, 4.1 mmol) in a 1:1 mixture of AcOH:water (4 mL) was heated in a sealed reaction vessel at 120° C. for 72 h. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure, diluted with 10 mL 10% aq. NaOH, and extracted with EtOAc (3×10 mL). The organic fractions were pooled, dried (Na2SO4), and concentrated under reduced pressure to provide 3-(benzyloxy)-1-(4-butylphenyl)pyridin-4(1H)-one, which was used in the subsequent step without further purification. LC/MS (M+H)+ 334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399651B2
Source datasetuspto-grants-2016_07
ORD IDord-bded7e666d9141fea1a87fab3292eef5
Source noteuspto-grants-2016_07