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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31387Erstellt: 23. Oktober 2026

Hydrochloric Acid → 2-(Chloromethylsulfonylamino)acetophenone

https://huagongshe.com/de/reaction/31387

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethylamineHCID 8471—
Edukt(Chloromethyl)sulfonyl chlorideHCID 77054—
EduktEthanone, 2-amino-1-phenyl-, hydrochloride (1:1)HCID 2723597—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(Chloromethylsulfonylamino)acetophenoneHCID 2302441776%

Reaktionsschritte

2-Aminoacetophenone hydrochloride (4.56 g, 26.6 mmol) was dissolved in dichloromethane (250 mL). To the solution was added triethylamine (9.30 mL, 66.7 mmol), and the mixture was stirred at room temperature for 10 minutes. After the reaction mixture was cooled to 0° C., chloromethanesulfonyl chloride (purity 90%, 3.60 mL, 36.3 mmol) was added to the mixture, and the mixture was stirred at the same temperature for 1 hour. 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 diethyl ether, and the deposited crystals were collected by filtration and dried to obtain 2-(chloromethylsulfonylamino)acetophenone (5.00 g, 76%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425636B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-c4419f48247f49d78d5729b8f6dd7492
Quellennotizuspto-grants-2008_09