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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845143Generated: November 1, 2026

4-chloro-N-methoxy-N-methyl-3-(methylsulfonyl)benzamide → 1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanone

https://huagongshe.com/reaction/1845143

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-N-methoxy-N-methyl-3-(methylsulfonyl)benzamideHCID 58107391—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanoneHCID 58188228—

Reaction Steps

A round bottom flask was charged with 4-chloro-N-methoxy-N-methyl-3-(methylsulfonyl)benzamide (18.0 g, 64.9 mmol) and tetrahydrofuran (200 mL) at 0° C. Methylmagnesiumbromide (1M solution in THF, 78 mL, 78 mmol) was added slowly and the reaction was stirred for 3 h at that temperature. The reaction was then quenched with aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layers were concentrated under reduced pressure and the residue was purified by flash chromatography to get the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946439B2
Source datasetuspto-grants-2015_02
ORD IDord-e187ae654982486094a513dcbf0ac83c
Source noteuspto-grants-2015_02