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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2226241Erstellt: 26. Oktober 2026

1-Bromo-1,1-difluoro-5-(t-butyl-dimethylsilyloxy)-2-pentyne → 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/2226241

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-1,1-difluoro-5-(t-butyl-dimethylsilyloxy)-2-pentyneHCID 15222237—
Edukt2-[(1S,2R,3R,5S)-2-(3,3-ethylenedioxyoctyl)-3-(tetrahydropyranyloxy)-5-(t-butylsiloxy)cyclopentyl]acetaldehydeHCID 123218162—
KatalysatorZincHCID 23994—
KatalysatorMercurous ChlorideHCID 24182—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-[(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—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05346921
Quelldatensatzuspto-grants-1994_09
ORD IDord-5ad531bf66084a17bdbcacc10f7a0af5
Quellennotizuspto-grants-1994_09