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HRID 1447579Erstellt: 25. Oktober 2026

Hydrochloric Acid → 17alpha-Chloroacetoxy-pregn-4-ene-3,20-dione

https://huagongshe.com/reaction/1447579

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTolueneHCID 1140—
Edukt17-HydroxyprogesteroneHCID 6238—
EduktTrifluoroacetic anhydrideHCID 9845—
LösungsmittelMethanolHCID 887—
Produkt17alpha-Chloroacetoxy-pregn-4-ene-3,20-dioneHCID 86736717—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of 3-/N,N-bis(2-chloroethyl)amino/-4-methylbenzoic acid (27.6 g) and trifluoroacetic anhydride (21.0 g) is heated under stirring at 60° C. for 15 min. To the mixture 17α-hydroxypregn-4-ene-3,20-dione (16.5 g) is added and the mixture is heated under stirring at 80° C. for 5 h. Toluene (150 ml) is added, the solution is filtered, and to the filtrate chloroform (200 ml) is added. After washing with H2O and aq. NaHCO3, drying, and evaporation an oil is obtained, to which a mixture of methanol (300 ml) and conc. HCl (3 ml) is added. After 16 h at room temperature the solution is evaporated and the residue chromatographed on a silica gel column using toluene/ethyl acetate (2:1) as eluent. The eluate fraction having Rf =0.40 gives 17α-/3-(N,N-bis(2-chloroethyl)amino)-4-methylbenzoyloxy/pregn-4-ene-3,20-dione (1, 6.8 g, m.p. 170°-1° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04177269
Quelldatensatzuspto-grants-1979_12
ORD IDord-72c0cc4976964636a99400b0f198c648
Quellennotizuspto-grants-1979_12