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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196297Generated: October 30, 2026

2-Nitrobenzenesulfonyl chloride → 2-(5-Bromo-2-fluorophenyl)-2-difluoromethyl-1-(2-nitro-benzenesulfonyl)-aziridine

https://huagongshe.com/reaction/2196297

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantPotassium BicarbonateHCID 516893—
Reactant2-Amino-2-(5-bromo-2-fluoro-phenyl)-3,3-difluoro-propan-1-olHCID 66666099—
SolventAcetonitrileHCID 6342—
Product2-(5-Bromo-2-fluorophenyl)-2-difluoromethyl-1-(2-nitro-benzenesulfonyl)-aziridineHCID 8665026737.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Amino-2-(5-bromo-2-fluoro-phenyl)-3,3-difluoro-propan-1-ol (13.04 g, 45.9 mmol) [examples 42 step d)] was dissolved in 261 mL acetonitrile, 2-nitrobenzenesulfonyl chloride (22.38 g, 101 mmol) and potassium hydrogencarbonate (13.79 g, 138 mmol) were added. The mixture was heated to 80° C. and stirred over night. After this period, the reaction mixture was cooled down and partitioned between saturated aqueous NaHCO3 solution and TBME. The layers were separated, washed with brine and TBME. The combined organic layers were dried over MgSO4.H2O and evaporated. The crude product was purified on a silica gel column by eluting with hexane/dichloromethane 2/1→1/2 to give 7.71 g of the title compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338413B1
Source datasetuspto-grants-2012_12
ORD IDord-80681f76ae8248beaf6dfd024dd71a15
Source noteuspto-grants-2012_12