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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371828Generated: October 30, 2026

p-Toluenesulfonic acid → 17beta,19-Dihydroxy-1alpha-methyl-4-androsten-3-one 3-ethylenethioketal

https://huagongshe.com/reaction/371828

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1,1-EthanedithiolHCID 33645—
Reactant17beta,19-Dihydroxy-1alphamethyl-4-androsten-3-oneHCID 22797425—
SolventAcetic AcidHCID 176—
Product17beta,19-Dihydroxy-1alpha-methyl-4-androsten-3-one 3-ethylenethioketalHCID 22797424—

Reaction Steps

17β,19-Dihydroxy-1α-methyl-4-androsten-3-one in acetic acid is treated with ethanedithiol and p-toluenesulfonic acid. After 4 hours at room temperature, the solution is poured onto water and the mixture extracted with methylenechloride. The methylenechloride extracts are washed well with water, sodium hydroxide solution, water, dried over sodium sulfate and evaporated under reduced pressure to leave 17β,19-dihydroxy-1α-methyl-4-androsten-3-one 3-ethylenethioketal which is recrystallized once from a solution of acetone-hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087524
Source datasetuspto-grants-1978_05
ORD IDord-70411f430a4740aa990002bf750fbbba
Source noteuspto-grants-1978_05