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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646812Generated: November 1, 2026

4-Bromophenacyl bromide → HCID 57222157, compound

https://huagongshe.com/reaction/1646812

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
ReactantPotassium CarbonateHCID 11430—
Reactant103187-09-3HCID 18397185—
SolventAcetoneHCID 180—
ProductHCID 57222157HCID 5722215799%

Reaction Steps

A mixture of (7R)-(+)-7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoic acid (0.71 g, 2.0 mmoles), p-bromophenacylbromide (0.56 g, 2.0 mmoles), and potassium carbonate (0.30 g, 2.2 mmole) in acetone (15 ml) was stirred for 2.5 hours at room temperature. After the reaction was completed, the solvent was evaporated in a reduced pressure, the residue was taken up in the isopropylether. Working up in the usual manner gave the crude product, which was chromatographed on silica gel column with isopropylether to give p-bromophenacyl (7R)-(+)-7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoate (1.09 g, 99%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180742
Source datasetuspto-grants-1993_01
ORD IDord-cae48b1503ee43cf9496d61cfd0c73a5
Source noteuspto-grants-1993_01