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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187475Generated: November 1, 2026

5-(Benzyloxy)-1-methyl-4-oxo-1,4-dihydropyridine-2-carboxylic acid → 3-(benzyloxy)-1-methylpyridin-4(1H)-one

https://huagongshe.com/reaction/1187475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Benzyloxy)-1-methyl-4-oxo-1,4-dihydropyridine-2-carboxylic acidHCID 15462295—
SolventDimethylformamideHCID 6228—
Product3-(benzyloxy)-1-methylpyridin-4(1H)-oneHCID 5105161394%

Reaction Conditions

Temperature135 °C

Reaction Steps

A suspension of 5-benzyloxy-1-methyl-4-oxo-1,4-dihydro-pyridine-2-carboxylic acid (18.2 g, 70.2 mmol) in 100 mL of DMF was stirred at oil bath temperature (130-140° C.) for 1.5 h. The reaction mixture was concentrated in vacuo, and the residual oil was diluted with dichloromethane (10 mL) and ethyl acetate (80 mL). The precipitated solid was collected by suction filtration to give 3-benzyloxy-1-methyl-1H-pyridin-4-one as a yellow powder (14.2 g, 94% yield). MS-ESI (m/z): 215.7 [M+1]+, 91.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673943B2
Source datasetuspto-grants-2014_03
ORD IDord-12816820571a4aea95da9907b5340223
Source noteuspto-grants-2014_03