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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221743Generated: November 1, 2026

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

https://huagongshe.com/reaction/221743

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 numberUS08207164B2
Source datasetuspto-grants-2012_06
ORD IDord-f51d69817a754bb9bb0c1befa82f8335
Source noteuspto-grants-2012_06