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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383360Generated: November 1, 2026

Potassium Carbonate → Tert-butyl4-({3-[(R)-cyclohexyl(hydroxy)phenylmethyl]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2383360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-(bromomethyl)piperidine-1-carboxylateHCID 15512811—
ReactantHCID 178519502HCID 178519502—
SolventDimethylformamideHCID 6228—
ProductTert-butyl4-({3-[(R)-cyclohexyl(hydroxy)phenylmethyl]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylateHCID 5914595651%

Reaction Conditions

Temperature70 °C

Reaction Steps

Tert-butyl 4-(bromomethyl)piperidine-1-carboxylate (6.75 g, 24.2 mmol) was dissolved in DMF (62 ml) and (R)-cyclohexyl(phenyl)1H-1,2,4-triazol-3-ylmethanol (Preparation 2, 5.2 g, 20 mmol) added, followed by potassium carbonate (5.58 g, 40.4 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. The residue was purified by column chromatography on silica gel eluting with ethyl acetate:heptane, (1:4 to 1:1, by volume) to furnish the title compound as a white foam, in 51% yield, 4.7 g (contains 10% of the other riazole regio-isomer).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263623B2
Source datasetuspto-grants-2012_09
ORD IDord-d078bd1511b84418998344ba5caae562
Source noteuspto-grants-2012_09