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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497270Generated: October 30, 2026

4-Bromobenzoyl chloride → 1-(4-Bromophenyl)-2-(3-fluoro-4-methylthiophenyl)ethanone

https://huagongshe.com/reaction/497270

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzoyl chlorideHCID 68515—
Reactant4-(Bromomethyl)-2-fluoro-1-(methylsulfanyl)benzeneHCID 22316819—
CatalystZincHCID 23994—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1-(4-Bromophenyl)-2-(3-fluoro-4-methylthiophenyl)ethanoneHCID 2231667673%

Reaction Steps

To the mixture of 4-bromobenzoyl chloride (10.81 g, 49.26 mmol), zinc (4.40 g, 67.24 mmol) and tetrakis(triphenylphosphine)palladium(0) (2.99 g, 2.586 mmol) in DME (250 mL) was added dropwise the solution of 4-(bromomethyl)-2-fluoro-1-(methylsulfanyl)benzene (12.16 g, 51.72 mmol) in DME (120 mL) at room temperature. After 2.5 hour, the mixture was filtered through celite, the filtrate was evaporated, diluted with ethyl acetate (300 mL), washed with water (100 mL), brine (100 mL), dried over sodium sulfate, and concentrated in vacuo. The residue was washed with ethyl acetate-isopropylether, to give the subtitle compound (12.16 g, 73% yield) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949536B2
Source datasetuspto-grants-2005_09
ORD IDord-4a3e1e7266e649fc8a008e8013d4ad17
Source noteuspto-grants-2005_09