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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21922Generated: October 25, 2026

HCID 15222237, compound → 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15222237HCID 15222237—
Reactant2-[(1S,2R,3R,5S)-2-(3,3-ethylenedioxyoctyl)-3-(tetrahydropyranyloxy)-5-(t-butylsiloxy)cyclopentyl]acetaldehydeHCID 123218162—
CatalystZincHCID 23994—
CatalystMercurous ChlorideHCID 24182—
SolventTetrahydrofuranHCID 8028—
Product1-[(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—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426115
Source datasetuspto-grants-1995_06
ORD IDord-03ea2f543c9c4c50826dfdd180319a84
Source noteuspto-grants-1995_06