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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 326183생성일: 2026년 10월 24일

Pyridine 4-methylbenzene-1-sulfonate → (5Z,13E)-(8R,9S,11R,12R,15S,16RS)-9-Chloro-11,15-dihydroxy-16,19-dimethyl-5,13,18-prostatrienoic Acid

https://huagongshe.com/ko/reaction/326183

반응식

참여 물질

역할이름HCID투입량
반응물Pyridine 4-methylbenzene-1-sulfonateHCID 161440—
반응물(5Z,13E)-(8R,9S,11R,-12R,15S,16RS)-9-chloro-11,15-bis(tetrahydropyran-2-yloxy)-16,19-dimethyl-5,13,18-prostatrienoic acidHCID 67859606—
용매EthanolHCID 702—
용매DichloromethaneHCID 6344—
생성물(5Z,13E)-(8R,9S,11R,12R,15S,16RS)-9-Chloro-11,15-dihydroxy-16,19-dimethyl-5,13,18-prostatrienoic AcidHCID 6785958842%

반응 단계

A solution of 144 mg of (5Z,13E)-(8R,9S,11R,12R,15S,16RS)-9-chloro-11,15-bis(tetrahydropyran-2-yloxy)-16,19-dimethyl-5,13,18-prostatrienoic acid in 2 ml of absolute ethanol was combined with 6.4 mg of pyridine p-toluenesulfonate and agitated for 5 days at room temperature under argon. The reaction mixture was then diluted with 100 ml of methylene chloride, washed twice with saturated sodium chloride solution, dried over magnesium sulfate, and evaporated to dryness under vacuum. The residue was purified by column chromatography on silica gel with hexane/50-100% ethyl acetate as the eluent, thus obtaining 42.5 mg of the desired carboxylic acid as a highly viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04444788
출처 데이터셋uspto-grants-1984_04
ORD IDord-c98d9cf42f884f8caf14e63d9f3ac74f
출처 메모uspto-grants-1984_04