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HRID 642933作成日:2026年10月25日

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/642933

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物FormaldehydeHCID 712—
反応物Sodium HydroxideHCID 14798—
反応物Acetic 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—
溶媒1,4-DioxaneHCID 31275—
生成物1-[4-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-5,5-bis-hydroxymethyl-tetrahydro-furan-2-yl]-1H-pyrimidine-2,4-dioneHCID 66772729—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07696345B2
出典データセットuspto-grants-2010_04
ORD IDord-06ada91244b84992a9a96ee57f14e80c
出典メモuspto-grants-2010_04