Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 352396Erstellt: 25. Oktober 2026

Water → 4-(Benzyloxy)benzene-1-sulfonyl chloride

https://huagongshe.com/reaction/352396

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktEthyl AcetateHCID 8857—
EduktThionyl ChlorideHCID 24386—
EduktBenzyl Phenyl EtherHCID 70352—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt4-(Benzyloxy)benzene-1-sulfonyl chlorideHCID 4738385—

Reaktionsschritte

To a suspension of 22.4 g (146 mmol) of sulfur trioxide/DMF complex in 60 mL of anhydrous 1,2-dichloroethane at room temperature, was added a solution of 30 g (162 mmol) of benzylphenyl ether in 30 mL of anhydrous 1,2-dichloroethane. The resulting mixture was warmed to reflux and maintained there for 1 hour, cooled to room temperature and 10.8 mL (146 mmol) of thionyl chloride added. The reaction was then warmed to 75 C for 1 hour, cooled in an ice bath, 50 mL of water slowly added, then ethyl acetate. The layers were separated, washed with saturated sodium bicarbonate, brine, dried with magnesium sulfate, filtered and stripped. The resulting solids were triturated with hexane to afford 24.5 g of pure 4-(Benzyloxy)benzenesulfonyl chloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06747027B1
Quelldatensatzuspto-grants-2004_06
ORD IDord-be569f83d1ea421887b5ea785b7a15d0
Quellennotizuspto-grants-2004_06