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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846227Generated: November 2, 2026

Triphenylphosphine → HCID 89964578, compound

https://huagongshe.com/reaction/1846227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Penten-1-OLHCID 13181—
Reactant2-Bromo-3-pyridinolHCID 23070—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 64982982HCID 64982982—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
ProductHCID 89964578HCID 89964578—

Reaction Conditions

Temperature50 °C

Reaction Steps

2-bromo-3-(pent-4-en-1-yloxy)pyridine. Diethyl azodicarboxylate (1 eq.) is added dropwise to a stirring mixture of 2-bromo-3-hydroxypyridine (0.92 eq,), pent-4-en-1-ol (0.92 eq), and PPh3 (1.1 eq) in THF (0.2 M) at 0° C. under a N2 atmosphere. The reaction mixture is warmed to 50° C. in an oil bath. Reaction progress is monitored by TLC until judged complete. The reaction mixture is cooled to ambient temperature and diluted with saturated NaHCO3 solution. The aqueous solution is extracted with EtOAc, and the organic layer is dried over Na2SO4 and concentrated. The compound that may be thus obtained is purified by column chromatography to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952009B2
Source datasetuspto-grants-2015_02
ORD IDord-a244e876f5da4ad3906c34304d0f9f91
Source noteuspto-grants-2015_02