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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19834Generated: October 26, 2026

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

https://huagongshe.com/reaction/19834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Trifluoromethoxy)phenylboronic acidHCID 2734386—
Reactant2-Bromomethyl-4-(2,3,4,6-tetra-O-acetyl-D-glucopyranos-1-yl)-benzonitrileHCID 67131410—
CatalystPalladium ChlorideHCID 24290—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
Product4-(beta-D-glucopyranos-1-yl)-2-(4-trifluoromethoxy-benzyl)-benzonitrileHCID 86618956—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745414B2
Source datasetuspto-grants-2010_06
ORD IDord-2978893eff4643ecbe663c6f7d435a8a
Source noteuspto-grants-2010_06