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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402043Generated: November 1, 2026

Acetone → 1-Bromo-3-(4-chlorophenyl)propan-2-one

https://huagongshe.com/reaction/2402043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrogen BromideHCID 260—
ReactantBromineHCID 24408—
Reactant1-(p-Chlorophenyl)acetoneHCID 79699—
SolventAcetic AcidHCID 176—
Product1-Bromo-3-(4-chlorophenyl)propan-2-oneHCID 1474885569.3%

Reaction Steps

To a solution of 1-(4-chlorophenyl)propan-2-one (25.0 g, 148 mmol) in acetic acid (37.9 mL) was added 48% aqueous HBr (19.0 mL, 168 mmol). A solution of bromine (16.3 mL, 316 mmol) in acetic acid (63.2 mL) was then added over 10 minutes and the resulting solution was stirred for 4 hours at room temperature. Acetone (190 mL) was added and the resulting solution was stirred at room temperature for 3 days. The reaction was concentrated in vacuo and the residue was taken up in DCM (300 mL) and brine (100 mL). The layers were separated and the aqueous layer was extracted with DCM (100 mL). The combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (ethyl acetate/hexanes=0/100→15/85) to give 25.4 grams of the title compound as a dark gray solid (69% yield). 1H NMR (400 MHz, CDCl3) δ: 7.34-7.31 (m, 2H), 7.18-7.15 (m, 2H), 3.94 (s, 2H), 3.91 (2, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796271B2
Source datasetuspto-grants-2014_08
ORD IDord-6d1b2e5cdb97479db93cdb6918703025
Source noteuspto-grants-2014_08