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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464516Generated: October 30, 2026

4-Bromophenacyl bromide → HCID 57222157, compound

https://huagongshe.com/reaction/1464516

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 numberUS05304658
Source datasetuspto-grants-1994_04
ORD IDord-65b75f8a374d4770ac90d3b6f986b6b0
Source noteuspto-grants-1994_04