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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222254Generated: October 30, 2026

Triphenylphosphine → HCID 58270746, compound

https://huagongshe.com/reaction/222254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 58270786HCID 58270786—
ReactantHCID 178418369HCID 178418369—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58270746HCID 5827074652.9%

Reaction Steps

To a mixture of pyridin-3-yl 4-hydroxypiperidine-1-carboxylate (300 mg), 5-phenyl-1H-tetrazole (217 mg), triphenyl phosphine (460 mg), and THF (3 mL) was added dropwise a 2.2 M solution of diethyl azodicarboxylate in toluene (0.8 mL), followed by stirring at room temperature overnight. The reaction liquid was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (chloroform/methanol=99/1 to 90/10), and purified again by silica gel column chromatography (hexane/ethyl acetate=70/30 to 0/100). To the purified product was added hexane/ethyl acetate, followed by stirring, and then the resulting solid was collected by filtration and dried to obtain pyridin-3-yl 4-(5-phenyl-2H-tetrazol-2-yl)piperidine-1-carboxylate (250 mg) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207199B2
Source datasetuspto-grants-2012_06
ORD IDord-8a5e6dfe2de1403ba1c51f9315cff52c
Source noteuspto-grants-2012_06