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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438401Generated: November 1, 2026

Methanesulfonyl chloride → HCID 21097534, compound

https://huagongshe.com/reaction/1438401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Bromo-2,6-difluoroanilineHCID 610191—
SolventPyridineHCID 1049—
ProductHCID 21097534HCID 2109753498.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 4-bromo-2,6-difluoroaniline (3.0 g, 14.4 mmol) in pyridine (20 ml) was added methanesulfonyl chloride (2.23 ml, 28.8 mmol) at room temperature. Then the mixture was stirred at 50° C. for 6 hours. After cooing to room temperature, the mixture was concentrated in vacuo. The resulting residue was dissolved in THF (40 ml). To this solution was added 2M aqueous sodium hydroxide solution (40 ml) and the reaction was stirred at room temperature for 4 hours. The mixture was acidified with 2M aqueous HCl solution and the whole was extracted with EtOAc. The organic layer was washed with 2M aqueous HCl solution, brine, and dried over sodium sulfate. After concentration in vacuo, the title compound (4.05 g, 98% yield) was obtained as orange solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622589B2
Source datasetuspto-grants-2009_11
ORD IDord-12cebce0356e445390e2d505c052f6b8
Source noteuspto-grants-2009_11