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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277246Generated: October 25, 2026

4-Nitrobenzenesulfonyl chloride → (2,2-Difluorocyclopropyl)methyl 4-nitrobenzenesulfonate

https://huagongshe.com/reaction/2277246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant(2,2-Difluorocyclopropyl)methanolHCID 2761401—
SolventTetrahydrofuranHCID 8028—
Product(2,2-Difluorocyclopropyl)methyl 4-nitrobenzenesulfonateHCID 8673131987%

Reaction Steps

To a solution of (2,2-difluorocyclopropyl)methanol (20.0 g) and triethylamine (32.2 mL) in THF (300 mL) was added 4-nitrobenzenesulfonyl chloride (41.0 g) at 0° C., and the mixture was stirred for 4 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (47.2 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-4c9643ebc5074a0989c13ac531fd70bc
Source noteuspto-grants-2015_09