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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356641Generated: October 26, 2026

Hydrochloric Acid → 2-(Vinylsulfonylamino)acetophenone

https://huagongshe.com/reaction/2356641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantEthanesulfonylchloride, 2-chloro-HCID 15385—
ReactantEthanone, 2-amino-1-phenyl-, hydrochloride (1:1)HCID 2723597—
SolventDichloromethaneHCID 6344—
Product2-(Vinylsulfonylamino)acetophenoneHCID 2302441632%

Reaction Steps

2-Aminoacetophenone hydrochloride (1.00 g, 5.85 mmol) was dissolved in dichloromethane (50 mL). To the solution was added triethylamine (2.50 mL, 17.9 mmol), and the mixture was stirred at room temperature for 10 minutes. After the reaction mixture was cooled to 0° C., chloroethanesulfonyl chloride (0.92 mL, 8.80 mmol) was added to the mixture, and the mixture was stirred at the same temperature for 15 minutes. To the reaction mixture was added 2 mol/L hydrochloric acid and the mixture was extracted with chloroform. The organic layer was washed with saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. To the residue was added a mixed solvent of ethyl acetate and n-hexane for crystallization to obtain 2-(vinylsulfonylamino)acetophenone (0.42 g, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759371B2
Source datasetuspto-grants-2010_07
ORD IDord-9ae7e2093acb459c8f0b8f156ad3bbd6
Source noteuspto-grants-2010_07