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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447579Generated: October 25, 2026

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

https://huagongshe.com/reaction/1447579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
Reactant17-HydroxyprogesteroneHCID 6238—
ReactantTrifluoroacetic anhydrideHCID 9845—
SolventMethanolHCID 887—
Product17alpha-Chloroacetoxy-pregn-4-ene-3,20-dioneHCID 86736717—

Reaction Conditions

Temperature60 °C

Reaction Steps

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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04177269
Source datasetuspto-grants-1979_12
ORD IDord-72c0cc4976964636a99400b0f198c648
Source noteuspto-grants-1979_12