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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284468Generated: October 25, 2026

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

https://huagongshe.com/reaction/2284468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Cyclopropylbenzeneboronic acidHCID 2849428—
Reactant2-Bromomethyl-4-(2,3,4,6-tetra-O-acetyl-D-glucopyranos-1-yl)-benzonitrileHCID 67131410—
Product2-(4-Cyclopropyl-benzyl)-4-(beta-D-glucopyranos-1-yl)-benzonitrileHCID 86656440—

Reaction Steps

An Ar filled flask is charged with 2-bromomethyl-4-(2,3,4,6-tetra-O-acetyl-D-glucopyranos-1-yl)-benzonitrile (1.60 g), 4-cyclopropyl-phenylboronic acid (1.0 g), potassium carbonate (1.85 g) and a degassed 3:1 mixture of 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 (4 mL). The resulting solution is stirred at ambient temperature for 1 h and then neutralized with 1M 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 numberUS09145434B2
Source datasetuspto-grants-2015_09
ORD IDord-4857005b79b84fc6b1f51dee2fc251a7
Source noteuspto-grants-2015_09