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HRID 1038355作成日:2026年10月27日

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

https://huagongshe.com/reaction/1038355

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-Cyclopropylbenzeneboronic acidHCID 2849428—
反応物2-Bromomethyl-4-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranos-1-yl)-benzonitrileHCID 86656435—
触媒Palladium ChlorideHCID 24290—
溶媒WaterHCID 962—
溶媒Sodium chloride; waterHCID 57417360—
生成物2-(4-Cyclopropyl-benzyl)-4-(beta-D-glucopyranos-1-yl)-benzonitrileHCID 86656440—

反応手順

An Ar filled flask is charged with a stir bar, 2-bromomethyl-4-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranos-1-yl)-benzonitrile (1.78 g), 4-cyclopropyl-phenylboronic acid (1.00 g), potassium carbonate (1.85 g) and a 3:1 mixture of degassed acetone and water (22 mL). The mixture is stirred at room temperature for 5 min, before it is cooled in an ice-bath. Then palladium dichloride (30 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 (20 mL) and treated with 4 M aqueous potassium hydroxide solution (3.8 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US08551957B2
出典データセットuspto-grants-2013_10
ORD IDord-e399a88068594a7b94e8d185670c551d
出典メモuspto-grants-2013_10