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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926037Generated: October 26, 2026

Dimethylformamide → 2-(Trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoate

https://huagongshe.com/reaction/926037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant2-(Trimethylsilyl)ethyl 3-(cyclopropylsulfamoyl)benzoateHCID 71238446—
SolventWaterHCID 962—
Product2-(Trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoateHCID 7123873787.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2.12 g of 2-(trimethylsilyl)ethyl 3-(cyclopropylsulfamoyl)benzoate, 1.45 g of ethyl 4-bromobutyrate, 2.57 g of potassium carbonate, and 21 mL of DMF was stirred at 80° C. overnight. To the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine in this order, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 2.48 g of 2-(trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoate as a colorless oily substance. ESI+: 456

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284295B2
Source datasetuspto-grants-2016_03
ORD IDord-bfbae0cf377c43cda65cebf021422f12
Source noteuspto-grants-2016_03