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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456439Generated: October 25, 2026

Triphenylphosphine → 4-[2-(2-Morpholin-4-yl-ethoxy)-phenyl]-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/456439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-MorpholinoethanolHCID 61163—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantTert-butyl 4-(2-hydroxyphenyl)piperazine-1-carboxylateHCID 11543684—
SolventTetrahydrofuranHCID 8028—
Product4-[2-(2-Morpholin-4-yl-ethoxy)-phenyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 1843676464%

Reaction Conditions

Temperature0 °C

Reaction Steps

Diisopropyl azodicarboxylate (0.48 mL, 2.4 mmol) was added dropwise to a stirred solution of 4-(2-hydroxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (0.56 g, 2 mmol), 2-morpholin-4-yl-ethanol (0.24 mL, 2 mmol) and triphenylphosphine (0.63 g, 2.4 mmol) in THF (20 mL) cooled to 0° C. The resulting solution was warmed to r.t. and stirred for about 16 hours. The solvent was removed in vacuo and the residue purified by silica gel chromatography (ethyl acetate) to afford the final compound (0.50 g, 64%) as a clear oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186715B2
Source datasetuspto-grants-2007_03
ORD IDord-a1e654ad91ad4cd192c716c8c40a3aaa
Source noteuspto-grants-2007_03