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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21922생성일: 2026년 10월 24일

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/ko/reaction/21922

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 번호US05426115
출처 데이터셋uspto-grants-1995_06
ORD IDord-03ea2f543c9c4c50826dfdd180319a84
출처 메모uspto-grants-1995_06