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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859793Generated: November 1, 2026

Triphenylphosphine → HCID 54451574, compound

https://huagongshe.com/reaction/1859793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant6-Hydroxy-3,4-dihydro-1(2H)-naphthalenoneHCID 4679494—
ReactantHCID 18626470HCID 18626470—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54451574HCID 5445157434.2%

Reaction Steps

A solution of 1-N-Boc-4-(2-hydroxyethyl)imidazole (1.06 g, 5.0 mmol), 6-hydroxytetralone (0.811 g, 5.0 mmol), and triphenylphosphine (1.44 g, 5.5 mmol) in 10 mL of freshly distilled THF was cooled in an ice bath for 10 minutes and then treated with neat diethyl azodicarboxylate (0.87 mL, 5.5 mmol) added via syringe through a rubber septum. The ice bath was permitted to melt and the reaction continued at room temperature for 5 hours. The solvent was removed in vacuo and the residue was chromatographed (silica gel, 500 g; 1:1, EtOAc:hexanes), and the pure fractions were pooled to afford 0.61 g (33%) of the title compound as a clear, colorless, viscous oil: CI-MS m/e 357 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528535B2
Source datasetuspto-grants-2003_03
ORD IDord-ed3ffcc3c1204f81a92a0bbec2fbf6eb
Source noteuspto-grants-2003_03