Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 477576Erstellt: 24. Oktober 2026

Acetic acid, 2-phenoxy-, ethyl ester → 1-Phenylsulfonyl-2-oxo-3-phenoxypropane

https://huagongshe.com/de/reaction/477576

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic acid, 2-phenoxy-, ethyl esterHCID 17365—
EduktMethyl phenyl sulfoneHCID 18369—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Phenylsulfonyl-2-oxo-3-phenoxypropaneHCID 15080405—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

n-Butyllithium (8.5 ml, 1.6M in hexane) was added at -72° C. to a solution of methylphenyl sulfone (2.14 g, 13.7 mmol) in 80 ml of tetrahydrofuran. The reaction mixture was then allowed to warm slowly to -20° C. and maintained at this temperature for 25 minutes. It was then recooled to -72° C. and ethyl phenoxyacetate (1.48 g, 8.22 mmol) was added dropwise. The cooling bath was removed, the mixture was stirred at 20° C. for 14 hrs. and then poured into 100 ml of saturated NH4Cl and extracted with diethyl ether. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulfate and the solvent removed under reduced pressure. The crude residue was purified by column chromatography (silica gel, methylene chloride) giving 1-phenylsulfonyl-2-oxo-3-phenoxypropane, the compound of formula (2a), 800 mg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04888358
Quelldatensatzuspto-grants-1989_12
ORD IDord-2cd40da7323a4651b90ebe714304744b
Quellennotizuspto-grants-1989_12