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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383382Generated: October 31, 2026

Potassium Carbonate → Benzyl 4-({3-[hydroxy(diphenyl)methyl]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2383382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzyl 4-(bromomethyl)piperidine-1-carboxylateHCID 2776274—
Reactantdiphenyl(1H-1,2,4-triazol-5-yl)methanolHCID 178519469—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-({3-[hydroxy(diphenyl)methyl]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylateHCID 5914596781%

Reaction Conditions

Temperature70 °C

Reaction Steps

Benzyl 4-(bromomethyl)piperidine-1-carboxylate (5 g, 16 mmol) was dissolved in dimethylformamide (40 ml) and diphenyl-(1H-[1,2,4]triazol-3-yl)-methanol (Tetrahedron: Asymmetry, 8(9), 1491-1500; 1997; 3.35 g, 13.65 mmol) added, followed by potassium carbonate (3.69 g, 26.7 mmol). After stirring at 70° C. for 18 hours the solvent was removed in vacuo, and the residue partitioned between ethyl acetate (150 ml) and water (150 mL). The organic layer was separated, dried over magnesium sulphate, filtered and the solvent removed in vacuo to furnish the title compound as a white solid in 81% yield, 5.2 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263623B2
Source datasetuspto-grants-2012_09
ORD IDord-d621d1001885485288657c889dd2af88
Source noteuspto-grants-2012_09