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HRID 64248作成日:2026年10月25日

Sodium Bicarbonate → allyl 3,4,6-tri-O-benzyl-beta-D-glucopyranoside

https://huagongshe.com/reaction/64248

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物Tri-O-benzyl-D-glucalHCID 11742644—
反応物Propan-2-one--dichloromethane (1/1)HCID 21584124—
反応物Potassium hydroxy sulfiteHCID 23707502—
溶媒WaterHCID 962—
生成物allyl 3,4,6-tri-O-benzyl-beta-D-glucopyranosideHCID 1102737750%

反応手順

3,4,6-tri-O-benzyl-D-glucal (7.2 g, 17.3 mmol) in CH2Cl2/acetone (2:1, 105 mL) and a saturated solution of NaHCO3 (100 mL) was added. The mixture was stirred vigorously while a solution of Oxone (21.2 g, 34.6 mmol) in water (150 mL) was added dropwise over 30 minutes. After 1.5 hours of vigorous stirring the layers were separated, and the aqueous layer was extracted with CH2Cl2 (2×150 mL). The organic solutions were combined, dried over MgSO4, filtered and concentrated. The residue was co-evaporated with toluene (3×10 mL), dissolved in allyl alcohol (25 mL) and stirred at room temperature overnight. The reaction mixture was purified on a silica gel column (80 g) using an ISCO automated chromatography system, eluting with a 0→60% gradient of ethyl acetate in heptane, to give allyl 3,4,6-tri-O-benzyl-β-D-glucopyranoside (4.2 g, 50%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447133B2
出典データセットuspto-grants-2016_09
ORD IDord-bba88a93227143cebe8f3aba0f22b6a6
出典メモuspto-grants-2016_09