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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55551Erstellt: 24. Oktober 2026

Thymidine → 5'-O-tert-Butyldimethylsilylthymidine

https://huagongshe.com/de/reaction/55551

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThymidineHCID 5789—
EduktTriethylamineHCID 8471—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5'-O-tert-ButyldimethylsilylthymidineHCID 1025125988,4%

Reaktionsschritte

5'-O-tert-Butyldimethylsilylthymidine (Compound 2, Table I) was prepared by dissolving thymidine (25 g, 0.10 mole), 4-N,N-dimethylaminopyridine (3.15 g, 0.026 mole) and triethylamine (13.5 g, 18.6 ml, 0.13 mole) in 200 ml of dry N,N-dimethylformamide under a stream of argon. 19.4 g (0.13 mol) tert-butyldimethylchlorosilane was added to the dissolved mixture, with the entire mixture then being stirred for six hours before evaporation of the solvent. The resulting gum was dissolved in 30 ml ethyl acetate and the solution extracted with 10 ml saturated sodium bicarbonate solution, 30 ml water and 30 ml brine. Following drying of the organic layer, the residue was purified by flash chromatography using dichloromethane/ethanol (50/1) as eluent. Evaporation of the product-containing fractions yielded 31.5 g of the desired 5'-O-tert-butyldimethylsilylthymidine as a white foam (86% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05625050
Quelldatensatzuspto-grants-1997_04
ORD IDord-d4b5a0253f064b57881e8da5d1fae4d0
Quellennotizuspto-grants-1997_04