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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669384Generated: November 2, 2026

Allyl bromide → HCID 67343897, compound

https://huagongshe.com/reaction/1669384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 136344252HCID 136344252—
SolventDimethylformamideHCID 6228—
ProductHCID 67343897HCID 67343897—

Reaction Steps

To a mixture of 0.71 g of 4-hydroxy-3-[3-[3-(methoxycarbonylmethoxy)phenyl]-1-oxo-2-propenyl]-1,6-dimethyl-2(1H)-pyridinone in 5 ml of dimethylformamide was added 0.09 g of sodium hydroxide (60% oily), and this was stirred at room temperature for 1 hour. 0.26 ml of allyl bromide was added, and this was stirred at room temperature overnight. The solvent was distilled off under reduced pressure, 5 ml of tetrahydrofuran was added, insolubles were filtered, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.30 g of 4-allyloxy-3-[3-[3-(methoxycarbonylmethoxy)phenyl]-1-oxo-2-propenyl]-1,6-dimethyl-2(1H)-pyridinone [Compound No. (1b)] as a pale yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989478B2
Source datasetuspto-grants-2011_08
ORD IDord-38ce46544811402490c4206356c858d2
Source noteuspto-grants-2011_08