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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 373606생성일: 2026년 10월 25일

HCID 15222237, 화합물 → 1-[(1R,2R,4S,5R)-2-tetrahydropyranyloxy-4-t-butylsilyloxy-5-(2(RS)-hydroxy-3,3-difluoro-7-t-butyldimethylsilyloxy-4-heptynyl}-cyclopentyl]-3,3-ethylenedioxy-octane

https://huagongshe.com/reaction/373606

반응식

참여 물질

역할이름HCID투입량
반응물HCID 15222237HCID 15222237—
반응물2-[(1S,2R,3R,5S)-2-(3,3-ethylenedioxyoctyl)-3-(tetrahydropyranyloxy)-5-(t-butylsiloxy)cyclopentyl]acetaldehydeHCID 123218162—
촉매ZincHCID 23994—
촉매Mercurous ChlorideHCID 24182—
용매TetrahydrofuranHCID 8028—
생성물1-[(1R,2R,4S,5R)-2-tetrahydropyranyloxy-4-t-butylsilyloxy-5-(2(RS)-hydroxy-3,3-difluoro-7-t-butyldimethylsilyloxy-4-heptynyl}-cyclopentyl]-3,3-ethylenedioxy-octaneHCID 123496017—

반응 단계

To a solution of 2-[(1S,2R,3R,5S)-2-(3,3-ethylenedioxyoctyl)-3-(tetrahydropyranyloxy)-5-(t-butylsiloxy)cyclopentyl]acetaldehyde (64) (1.00 g) in THF (25 ml) was added activated zinc powder (2.54 g), and while cooling on ice, the solution of 1-bromo-1,1-difluoro-5-(t-butyl-dimethylsilyloxy)-2-pentyne (i) (0.92 g) in THF (5 ml) was added dropwise to the resultant mixture. To the resultant solution was added mercury chloride (0.11 g) and the resultant mixture was stirred under ultrasonic irradiation. The reaction mixture was treated in the conventional manner and the obtained crude product was subjected to silica gel column chromatography to give the title compound (65).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05164415
출처 데이터셋uspto-grants-1992_11
ORD IDord-0dfc62e697574e8c95a78ae3665f93a7
출처 메모uspto-grants-1992_11