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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926036Generated: October 25, 2026

Cyclopropylamine → 2-(Trimethylsilyl)ethyl 3-(cyclopropylsulfamoyl)benzoate

https://huagongshe.com/reaction/926036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
Reactant2-(Trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoateHCID 86676334—
SolventPyridineHCID 1049—
Product2-(Trimethylsilyl)ethyl 3-(cyclopropylsulfamoyl)benzoateHCID 71238446—

Reaction Steps

A mixture of 2.00 g of 2-(trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoate, 1.2 mL of cyclopropylamine, and 20 mL of pyridine was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and to the residue was added an aqueous citric acid solution, followed by extraction with ethyl acetate. The organic layer was washed with 1.0 M hydrochloric acid and saturated brine in this order, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 2.12 g of 2-(trimethylsilyl)ethyl 3-(cyclopropylsulfamoyl)benzoate as a pale yellow oily substance. EI: 341

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284295B2
Source datasetuspto-grants-2016_03
ORD IDord-6fa33e7314ef46d3a15ac7c4d5e5fa02
Source noteuspto-grants-2016_03