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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31388Erstellt: 23. Oktober 2026

Hydrochloric Acid → 2-(Vinylsulfonylamino)acetophenone

https://huagongshe.com/de/reaction/31388

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethylamineHCID 8471—
EduktEthanesulfonylchloride, 2-chloro-HCID 15385—
EduktEthanone, 2-amino-1-phenyl-, hydrochloride (1:1)HCID 2723597—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(Vinylsulfonylamino)acetophenoneHCID 2302441632%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425636B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-584e886578ee47e49264f1a5929a0d1c
Quellennotizuspto-grants-2008_09