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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108764Generated: October 30, 2026

Bromomethyl 4-methoxyphenyl ketone → HCID 18784184, compound

https://huagongshe.com/reaction/1108764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
ReactantEthyl AcetoacetateHCID 8868—
ReactantPotassium tert-butoxideHCID 23665647—
SolventBenzeneHCID 241—
ProductHCID 18784184HCID 1878418487%

Reaction Steps

After adding potassium tert-butoxide to a solution of ethyl acetoacetate (25.7 g) in benzene (420 ml) while cooling on ice, 4-methoxyphenacyl bromide (24.8 g) was gradually added and the mixture was refluxed for an hour. After allowing the reaction solution to cool, it was washed with 5% sodium hydroxide and purified water, and dried with anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to give 26.2 g of ethyl 2-[2-(4-methoxyphenyl)-2-oxoethyl]-4-oxopentanoate (87.0% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069176
Source datasetuspto-grants-2000_05
ORD IDord-cd529ceff3754de6a072eea152387e45
Source noteuspto-grants-2000_05