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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624513Generated: October 29, 2026

Thionyl Chloride → N-[1-(4-Bromo-phenyl)-cyclopropanecarbonyl]-methanesulfonamide

https://huagongshe.com/reaction/1624513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium hydrideHCID 24758—
ReactantMethanesulfonamideHCID 72879—
Reactant1-(4-Bromophenyl)cyclopropane-1-carboxylic acidHCID 16227966—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN-[1-(4-Bromo-phenyl)-cyclopropanecarbonyl]-methanesulfonamideHCID 6657740686.1%

Reaction Steps

1-(4-Bromo-phenyl)-cyclopropanecarboxylic acid (22 g, 91.3 mmol) and SOCl2 (13.6 mL, 183 mmol) in CH2Cl2 were heated together for 1.5 hours then evaporated to afford a dark oil. This oil was added via syringe over 30 minutes to a mixture of MeSO2NH2 (19 g, 200 mmol) in THF (250 mL) that was pre-treated at room temperature with NaH (60% in oil; 8.0 g, 200 mmol) for 1.5 hours. After a further 20 minutes, the mixture was poured into water, acidified and extracted with CH2Cl2, washed with water (2×) and evaporated to ˜100 mL. Hexane (300 mL) was added and the product collected by filtration to yield the title compound (25 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778983B2
Source datasetuspto-grants-2014_07
ORD IDord-f0e4548fc02b47cb98a9438e42eb402d
Source noteuspto-grants-2014_07