Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2394804Erstellt: 25. Oktober 2026

Benzaldehyde → N-(alpha-phenylsulphonyl-benzyl)benzamide

https://huagongshe.com/reaction/2394804

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktMethanolHCID 887—
EduktBenzamideHCID 2331—
EduktBenzenesulfinic acid, sodium saltHCID 2723840—
LösungsmittelFormic AcidHCID 284—
LösungsmittelWaterHCID 962—
ProduktN-(alpha-phenylsulphonyl-benzyl)benzamideHCID 1897435515,6%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

A solution of 40.2 g of sodium phenylsulphinate in 200 cm3 of water is introduced into a 500 cm3 reactor equipped with a magnetic stirrer and a reflux condenser. A mixture of 12.35 g of benzamide and 21.22 g of benzaldehyde is then added. 60 cm3 of methanol are then added so as to obtain an off-white emulsion and then 7.54 cm3 of formic acid (d=1.22) are added. After stirring for 41 hours 30 minutes at a temperature in the region of 20° C., the mixture is heated for 3 hours at 65° C. After filtration through sintered glass No. 4, the product obtained is washed with twice 15 cm3 of isopropyl ether and then with twice 15 cm3 of water. After drying, there are obtained, with a yield of 15.6%, 5.48 g of N-(α-phenylsulphonyl-benzyl)benzamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05811550
Quelldatensatzuspto-grants-1998_09
ORD IDord-fff0801a5bd2497aa76faa86410e4194
Quellennotizuspto-grants-1998_09