돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 463532생성일: 2026년 10월 24일

Deoxycholic Acid → 12alpha-Hydroxy-3-oxo-5beta-cholan-24-oic Acid

https://huagongshe.com/ko/reaction/463532

반응식

참여 물질

역할이름HCID투입량
반응물Deoxycholic AcidHCID 222528—
용매Chloroform ethanolHCID 21889567—
생성물12alpha-Hydroxy-3-oxo-5beta-cholan-24-oic AcidHCID 16073825.9%

반응 단계

The above mixture of oxidation products of deoxycholic acid (310 mg) resulted from the eluate of chloroform-ethanol (97:3, v/v) was dissolved in a small amount of chloroform-ethanol (99:1, v/v) and the solution was absorbed on silica gel (20 g) column. The column was eluted with chloroform-ethanol (98:2, v/v) and then with chloroform-ethanol (97:3, v/v). Each 10 ml portions of the eluate was collected in a fraction tube. Fractions which showed a corresponding single spot by thin layer chromatography were combined and the solvent was distilled off by a rotary evaporator. As the results, 12α-hydroxy-3-keto-5β-cholanic acid (80 mg) was obtained from the first half of the fractions eluted with chloroform-ethanol (98:2, v/v) and 12α-hydroxy-3-keto-4-cholenic acid (10 mg) was obtained from the latter half thereof. 12α-Hydroxy-3-keto-5β-pregnan-20α-carboxylic acid (5 mg) was obtained from the first half of the fractions eluted with chloroform-ethanol (97:3, v/v) and 12α-hydroxy-3-keto-chola-1,4 -dienic acid (10 mg) was obtained from the latter half thereof.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04520102
출처 데이터셋uspto-grants-1985_05
ORD IDord-69030becfde94377ac2b52cf29dee9fe
출처 메모uspto-grants-1985_05