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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55551생성일: 2026년 10월 25일

Thymidine → 5'-O-tert-Butyldimethylsilylthymidine

https://huagongshe.com/reaction/55551

반응식

참여 물질

역할이름HCID투입량
반응물ThymidineHCID 5789—
반응물TriethylamineHCID 8471—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물5'-O-tert-ButyldimethylsilylthymidineHCID 1025125988.4%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05625050
출처 데이터셋uspto-grants-1997_04
ORD IDord-d4b5a0253f064b57881e8da5d1fae4d0
출처 메모uspto-grants-1997_04