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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65345생성일: 2026년 10월 24일

Acetone → Anecortave Acetate

https://huagongshe.com/ko/reaction/65345

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Potassium bisulfateHCID 516920—
반응물17alpha-Hydroxy-20-phenoxypregna-4,9(11),20-trien-3-oneHCID 13823825—
반응물Potassium hydroxy sulfiteHCID 23707502—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Anecortave AcetateHCID 111332—

반응 조건

온도15 °C

반응 단계

17α-hydroxy-20-phenoxypregna-4,9(11),20-trien-3-one (4.05 grams, 10 mmoles) is slurried in a 250 ml round bottom flask, in an aqueous pH 8 potassium phosphate buffer (20 ml, 0.05M in PO4≡) prepared as in Example 1. Tetra n-butylammonium bromide (0.64 grams, 2.0 mmole), acetone (20 ml), methylene chloride (40 ml) are added and the mixture cooled to 15° C. 18.42 grams, 30 mmoles of OXONE® (2KHSO5.KHSO4.K2SO4) is dissolved in 62 ml of water filtered and placed in an addition funnel. The OXONE solution is added dropwise with stirring while maintaining the pH between 6.8 and 7.2 with 30% potassium hydroxide. The reaction is run to completion. Fifty ml of water is added and the reaction mixture is filtered. The filtered solids are rinsed with methylene chloride and water, the layers are separated and the methylene chloride layer is filtered thru a solka flok filter. Two ml of glacial acetic acid are added and the mixture is stirred for 1 hour to yield 2.5 grams of 17α-hydroxy-21 -acetoxy-pregna-4,9(11)-diene-3,20-dione at room temperature.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04613463
출처 데이터셋uspto-grants-1986_09
ORD IDord-d1cbf3bc997146c8ba55f3de17402c48
출처 메모uspto-grants-1986_09