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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038355Generated: October 25, 2026

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

https://huagongshe.com/reaction/1038355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Cyclopropylbenzeneboronic acidHCID 2849428—
Reactant2-Bromomethyl-4-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranos-1-yl)-benzonitrileHCID 86656435—
CatalystPalladium ChlorideHCID 24290—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
Product2-(4-Cyclopropyl-benzyl)-4-(beta-D-glucopyranos-1-yl)-benzonitrileHCID 86656440—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551957B2
Source datasetuspto-grants-2013_10
ORD IDord-e399a88068594a7b94e8d185670c551d
Source noteuspto-grants-2013_10