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HRID 21922作成日:2026年10月25日

HCID 15222237、化合物 → 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/21922

反応式

関与物質

役割名称HCID仕込み量
反応物HCID 15222237HCID 15222237—
反応物2-[(1S,2R,3R,5S)-2-(3,3-ethylenedioxyoctyl)-3-(tetrahydropyranyloxy)-5-(t-butylsiloxy)cyclopentyl]acetaldehydeHCID 123218162—
触媒ZincHCID 23994—
触媒Mercurous ChlorideHCID 24182—
溶媒TetrahydrofuranHCID 8028—
生成物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-octaneHCID 123496017—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426115
出典データセットuspto-grants-1995_06
ORD IDord-03ea2f543c9c4c50826dfdd180319a84
出典メモuspto-grants-1995_06