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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1645303생성일: 2026년 10월 26일

Acetic Acid → 1-[4-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-5,5-bis-hydroxymethyl-tetrahydro-furan-2-yl]-1H-pyrimidine-2,4-dione

https://huagongshe.com/reaction/1645303

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물FormaldehydeHCID 712—
반응물Sodium HydroxideHCID 14798—
반응물Acetic Acid 4-(tert-butyl-diphenyl-silanyloxy)-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-5-formyl-tetrahydro-furan-3-yl EsterHCID 86594161—
용매1,4-DioxaneHCID 31275—
생성물1-[4-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-5,5-bis-hydroxymethyl-tetrahydro-furan-2-yl]-1H-pyrimidine-2,4-dioneHCID 66772729—

반응 단계

Hydroxymethylation of the 5′-aldehyde is performed as per the method of Cannizzaro which is well documented in the literature (Jones, G. H., et. al., J. Org. Chem. 1979, 44, 1309-1317). These conditions are expected to additionally remove the 2′-O-acetyl group. Generally, Briefly, formaldehyde (2.0 eq., 37% aq.) and NaOH (1.2 eq., 2 M) is added to a solution of Compound 10 in 1,4-dioxane. After stirring at room temperature for several hours, this mixture is neutralized with acetic acid, evaporated to dryness, suspended in methanol, and evaporated onto silica gel. The resulting mixture is added to the top of a silica gel column and eluted using an appropriate solvent system to give Compound 11.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08124745B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-981b06269c9643f68fe386725b283c87
출처 메모uspto-grants-2012_02