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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713498Generated: October 25, 2026

Triethylamine → N-cyclopropyl-2-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1713498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantCyclopropylamineHCID 69828—
SolventTetrahydrofuranHCID 8028—
ProductN-cyclopropyl-2-nitrobenzenesulfonamideHCID 79663087%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of cyclopropylamine (1.0 g, 18 mmol) and triethylamine (3.7 mL, 27 mmol) in tetrahydrofuran (20 mL) was added 2-nitrobenzenesulfonyl chloride (3.9 g, 18 mmol) at 0° C., and the mixture was stirred at 0° C. for 1 hour. The solvent was distilled off under reduced pressure, and the residue was diluted with ethyl acetate. The reaction solution was washed with water and saturated brine and dried over magnesium sulfate. The solid was filtered off, and the filtrate was concentrated. The residue was purified with silica gel column chromatography (hexane:ethyl acetate=1:1) and concentrated. The residue was washed with hexane and collected by filtration to obtain the title compound (3.7 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795267B2
Source datasetuspto-grants-2010_09
ORD IDord-54aa42dedd6945a3ae83e85f9e326f61
Source noteuspto-grants-2010_09