Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2050767Erstellt: 26. Oktober 2026

Acetic Acid → Ethyl 3-phenyl-2-(tert.butylaminosulfonyl)prop-2-enoate

https://huagongshe.com/reaction/2050767

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktBenzaldehydeHCID 240—
EduktAmmonium AcetateHCID 517165—
Eduktethyl-2-(N-tert-butylsulfamoyl)acetateHCID 19833529—
ProduktEthyl 3-phenyl-2-(tert.butylaminosulfonyl)prop-2-enoateHCID 5703702172%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

11.2 g (0.05 mol) of ethyl 2-(tert.butylaminosulfonyl)acetate (see J. Org. Chem. 43, p. 4535 (1978)) are dissolved in 50 ml of benzaldehyde, 2 g of ammonium acetate and 2 ml of glacial acetic acid are added, and the mixture is stirred for 2 hours at 60° C. under a water pump vacuum (20 mm). The excess aldehyde is subsequently distilled off, and the residue is digested using n-hexane and recrystallized from isopropanol. 11.2 g (72% of theory) of ethyl 3-phenyl-2-(tert.butylaminosulfonyl)prop-2-enoate of melting point 111°-113° C. are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05015284
Quelldatensatzuspto-grants-1991_05
ORD IDord-50e92ea2e822489f80998c8691832cdf
Quellennotizuspto-grants-1991_05