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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605815Generated: November 1, 2026

Triphenylphosphine → HCID 67067066, compound

https://huagongshe.com/reaction/605815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Chlorobenzyl alcoholHCID 70117—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 67067074HCID 67067074—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67067066HCID 6706706662.8%

Reaction Steps

A THF (5 ml) solution containing 3-pyridyl 4-(4-hydroxybenzoyl)-1-piperazinecarboxylate (300 mg) and diethyl azodicarboxylate (0.62 ml, 40% Tol solution) was dropwise added to a THF (5 ml) solution containing 3-chlorobenzyl alcohol (200 mg) and triphenylphosphine (360 mg), at 0° C., followed by stirring at room temperature for 3 days. The reaction solution was diluted with chloroform, washed with an aqueous saturated sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform:methanol=95:5 (v/v)), and the resulting solid was recrystallized from 2-propanol to obtain 3-pyridyl 4-{4-[(3-chlorobenzoyl)oxy]benzyl}-1-piperazinecarboxylate (260 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915261B2
Source datasetuspto-grants-2011_03
ORD IDord-475661e44faf409a90e6d0020b3a4e7e
Source noteuspto-grants-2011_03