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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65343Generated: October 25, 2026

Edetate Sodium → 17alpha-Hydroxy-20,21-epoxy-20-phenoxypregna-4,9(11)-diene-3-one

https://huagongshe.com/reaction/65343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEdetate SodiumHCID 6144—
ReactantPotassium HydroxideHCID 14797—
ReactantPotassium bisulfateHCID 516920—
Reactant17alpha-Hydroxy-20-phenoxypregna-4,9(11),20-trien-3-oneHCID 13823825—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventPotassium Phosphate, TribasicHCID 62657—
Product17alpha-Hydroxy-20,21-epoxy-20-phenoxypregna-4,9(11)-diene-3-oneHCID 56624370—

Reaction Steps

17α-hydroxy-20-phenoxypregna-4,9(11),20-trien-3-one (4.04 grams, 10 mmoles) is slurried in pH 8 potassium phosphate buffer (50 ml, 0.02M PO4 57 ), 40 ml methylene chloride, 0.222 grams (1 mmole), of Ansul ether 181 (C10H22O5) and 20 ml acetone and the two phase mixture heated to 25° C. and adjusted to pH 8.5 with 30% potassium hydroxide. 18.4 grams, 30 mmoles of OXONE® (2KHSO5.KHSO4.K2SO4) is dissolved in 90 ml of water and 10 ml of a 5% by weight solution of Na4EDTA and the resulting solution added dropwise at 25° C. with vigorous agitation while maintaining the pH at 8.0-8.5 with 30% potassium hydroxide. When the reaction is complete the phases are separated hot and the aqueous phase extracted twice with 50 ml of methylene chloride. The combined organics are washed twice with 100 ml of aqueous 5% sodium hydroxide and clarified thru a solka flok filter and concentrated on a rotary evaporator to yield 17α-hydroxy-20,21-epoxy-20-phenoxypregna-4,9(11)-diene-3-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613463
Source datasetuspto-grants-1986_09
ORD IDord-f6162b161d614a6b80ca3cfa04173ed9
Source noteuspto-grants-1986_09