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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222240Generated: October 25, 2026

Tert-butyl 4-hydroxypiperidine-1-carboxylate → 1-(1-Tert-butoxycarbonylpiperidin-4-yl)-3-phenylpyrazole

https://huagongshe.com/reaction/222240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantCyanomethylenetributylphosphoraneHCID 4622928—
ReactantHCID 178420101HCID 178420101—
SolventTolueneHCID 1140—
Product1-(1-Tert-butoxycarbonylpiperidin-4-yl)-3-phenylpyrazoleHCID 5795204369.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-phenyl-1H-pyrazole (300 mg) in toluene (15 mL) were added tert-butyl 4-hydroxypiperidine-1-carboxylate (838 mg) and (tributylphosphoranylidene)acetonitrile (1.0 g), followed by stirring at 100° C. for 4 hours. The reaction liquid was concentrated under reduced pressure, and then the residue was purified by silica gel column chromatography (hexane/ethyl acetate=100/0 to 50/50) and purified again by silica gel column chromatography (hexane/ethyl acetate=100/0 to 70/30) to obtain tert-butyl 4-(3-phenyl-1H-pyrazol-1-yl)piperidine-1-carboxylate (475 mg) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207199B2
Source datasetuspto-grants-2012_06
ORD IDord-1bb9cfa8fe244eb3a2aceaf65e188cb8
Source noteuspto-grants-2012_06