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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65343생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/65343

반응식

참여 물질

역할이름HCID투입량
반응물Edetate SodiumHCID 6144—
반응물Potassium HydroxideHCID 14797—
반응물Potassium bisulfateHCID 516920—
반응물17alpha-Hydroxy-20-phenoxypregna-4,9(11),20-trien-3-oneHCID 13823825—
반응물Potassium hydroxy sulfiteHCID 23707502—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
용매Potassium Phosphate, TribasicHCID 62657—
생성물17alpha-Hydroxy-20,21-epoxy-20-phenoxypregna-4,9(11)-diene-3-oneHCID 56624370—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04613463
출처 데이터셋uspto-grants-1986_09
ORD IDord-f6162b161d614a6b80ca3cfa04173ed9
출처 메모uspto-grants-1986_09