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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643431Generated: November 2, 2026

Triphenylphosphine → Tert-butyl 4-(pyridin-4-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1643431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantHCID 178418642HCID 178418642—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(pyridin-4-yloxy)piperidine-1-carboxylateHCID 21906087—

Reaction Conditions

Temperature55 °C

Reaction Steps

tert-Butyl 4-hydroxypiperidine-1-carboxylate (6.348 g, 31.546 mmol) and triphenylphosphine (10.256 g, 39.432 mmol) were added to a solution of 4-hydroxypyridine (3 g, 31.456 mmol) in tetrahydrofuran (50 ml) at room temperature. Diisopropyl azodicarboxylate (7.66 ml, 39.432 mmol) was subsequently added dropwise and the mixture was then stirred at 55° C. for 15 h. Saturated sodium bicarbonate solution (50 ml) was added to the reaction mixture and the mixture was extracted with ethyl acetate (4×80 ml). The combined organic phases were washed with sat. sodium chloride solution (20 ml), dried over sodium sulfate and concentrated in vacuo. The crude product was subsequently purified by column chromatography (silica gel) with ethyl acetate/hexane (4:1). Yield: 4.11 g (46%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119805B2
Source datasetuspto-grants-2012_02
ORD IDord-7aa7cbaf96dc4cfaa39244cdaf7faca4
Source noteuspto-grants-2012_02