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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30358Generated: October 27, 2026

1-Chloro-4-(chloromethyl)benzene → 3-(3-Bromophenyl)-4-(4-chlorophenyl)-3-methyl-2-butanone

https://huagongshe.com/reaction/30358

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantEthyl AcetateHCID 8857—
ReactantCaesium hydroxide--water (1/1/1)HCID 23679066—
Reactant3-(3-Bromophenyl)butan-2-oneHCID 66436791—
CatalystTetrabutylammonium IodideHCID 67553—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-(3-Bromophenyl)-4-(4-chlorophenyl)-3-methyl-2-butanoneHCID 68675648—

Reaction Steps

To a solution of 3-(3-bromophenyl)-2-butanone (2.0 g, 8.8 mmol) in methylene chloride (100 mL) was added 4-chlorobenzyl chloride (1.4 g, 8.8 mmol), tetrabutylammonium iodide (0.16 g, 0.44 mmol) and cesium hydroxide monohydrate (5.9 g, 35 mmol). After stirring at room temperature for 3.5 h, the reaction mixture was poured into ethyl acetate (100 mL) and water (100 mL). The organic layer was separated and the aqueous layer extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered, and concentrated to dryness to give the title compound. 1H NMR (400 MHz, CD3OD): δ 7.5-7.1 (m, 4 H), 7.08 (d, 2H), 6.68 (d, 2H), 3.16 (ABq, 2H), 1.98 (s, 3H), 1.42 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423067B2
Source datasetuspto-grants-2008_09
ORD IDord-b7583f5efae64ba4bc4392e03243ee37
Source noteuspto-grants-2008_09