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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604962Generated: October 31, 2026

Phenacyl bromide → 722516-74-7

https://huagongshe.com/reaction/604962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzoic acid, 3-mercapto-HCID 95737—
SolventEthanolHCID 702—
Product722516-74-7HCID 59658539120.3%

Reaction Steps

To bromoacetophenone (250 mg, 1.16 mmole) and anhydrous K2CO3 (694 mg, 5.02 mmole) in ethanol, 193.6 mg (1.25 mmole) 3-mercaptobenzoic acid was added and the mixture refluxed overnight. The solvent was evaporated and water added to the solid residue. The basic aqueous solution was extracted with ethyl acetate to remove unreacted bromoacetophenone. The aqueous layer was acidified and extracted with ethyl acetate, dried, evaporated and the residue purified by flash chromatography using chloroform:methanol 95:5. Evaporation of the fractions resulted in a yellow powder (380 mg). M.S. m/s 271 (M−1)+. 1H NMR (DMSO) δ4.75 (2H, s, —CH2-), 7.39-7.7 (4H, m, 4×ArH), 7.75 (1H, d, ArH, J==5.61 Hz), 7.86 (1H, s, ArH), 8.02 (3H, d, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910770B2
Source datasetuspto-grants-2011_03
ORD IDord-69bb0a700ef84ad6b4751ec9bcb9dda1
Source noteuspto-grants-2011_03