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HRID 19834作成日:2026年10月26日

Acetone → 4-(beta-D-glucopyranos-1-yl)-2-(4-trifluoromethoxy-benzyl)-benzonitrile

https://huagongshe.com/reaction/19834

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Potassium CarbonateHCID 11430—
反応物4-(Trifluoromethoxy)phenylboronic acidHCID 2734386—
反応物2-Bromomethyl-4-(2,3,4,6-tetra-O-acetyl-D-glucopyranos-1-yl)-benzonitrileHCID 67131410—
触媒Palladium ChlorideHCID 24290—
溶媒WaterHCID 962—
溶媒Sodium chloride; waterHCID 57417360—
生成物4-(beta-D-glucopyranos-1-yl)-2-(4-trifluoromethoxy-benzyl)-benzonitrileHCID 86618956—

反応手順

An Ar filled flask is charged with 2-bromomethyl-4-(2,3,4,6-tetra-O-acetyl-D-glucopyranos-1-yl)-benzonitrile (0.25 g), 4-trifluoromethoxy-phenylboronic acid (0.20 g), potassium carbonate (0.26) and a 3:1 mixture of degassed acetone and water (4 mL). The mixture is stirred at room temperature for 5 min, before it is cooled in an ice-bath. Then palladium dichloride (5 mg) is added and the reaction mixture is stirred for 16 h at ambient temperature. The mixture is then diluted with brine and extracted with ethyl acetate. The combined extracts are dried over sodium sulfate and the solvent is removed under reduced pressure. The residue is dissolved in methanol (9 mL) and treated with 4 M aqueous potassium hydroxide solution (1 mL). The resulting solution is stirred at ambient temperature for 1 h and then neutralized with 1 M hydrochloric acid. The methanol is evaporated, and the residue is diluted with brine and extracted with ethyl acetate. The organic extracts collected are dried over sodium sulfate, and the solvent is removed. The residue is chromatographed on silica gel (dichloromethane/methanol 1:0->8:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745414B2
出典データセットuspto-grants-2010_06
ORD IDord-2978893eff4643ecbe663c6f7d435a8a
出典メモuspto-grants-2010_06