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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246754Generated: October 26, 2026

Triphenylphosphine → 1-Boc-4-(2-pyridyloxy)piperidine

https://huagongshe.com/reaction/1246754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantHCID 178516071HCID 178516071—
SolventTetrahydrofuranHCID 8028—
Product1-Boc-4-(2-pyridyloxy)piperidineHCID 21906039—

Reaction Steps

To a solution of 2-hydroxypyridine (2.0 g), tert-butyl 4-hydroxy-1-piperidinecarboxylate (5.3 g) and triphenylphosphine (8.3 g) in tetrahydrofuran (63 ml) was slowly added diethyl azodicarboxylate (5.5 g) at 8° C., and the mixture was stirred at room temperature for 4 hours. The reaction mixture was concentrated in vacuo to give the crude product of the title compound and the crude product was purified by chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129243B2
Source datasetuspto-grants-2006_10
ORD IDord-c8d9c4749fb54a3599bbfd5cec6c6a38
Source noteuspto-grants-2006_10