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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792986Generated: October 25, 2026

Triphenylphosphine → HCID 22024880, compound

https://huagongshe.com/reaction/1792986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant1-(4-Fluorophenyl)-2-(piperazin-1-yl)ethan-1-oneHCID 16769083—
Reactant4-Hydroxymethyl-2,6-bis-pentyloxyphenolHCID 22024906—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22024880HCID 2202488015.9%

Reaction Steps

To the solution of 4-hydroxymethyl-2,6-bis-pentyloxyphenol (525 mg, 1.62 mmol), 1-(4-fluorophenyl)-2-piperazine-1-yl-ethanone (432 mg, 1.94 mmol) and PPh3 (509 mg, 1.94 mmol) in drying THF (10 ml) was dropped diethyl azodicarboxylate (0.38 ml, 2.43 mmol) at 0° C. and then was stirred 15 minutes at room temperature. The solution was added with H2O, then CH2Cl2 was evaporated in vacuo and was washed with brine. The obtained organic solution was dried over anhydrous magnesium sulfate and filtered. The obtained filterate was vacuum concentrated to give the residue, which was purified by column chromatography (Hexane:EtOAc=1:10), yielding 129 mg (15%) of 1-(4-fluorophenyl)-2-[4-(4-hydroxy -3,5-bis-pentyloxybenzyl)piperizine-1-yl]ethanone as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078407B2
Source datasetuspto-grants-2006_07
ORD IDord-775e1765b7fa43c09871eef7ae04f3c2
Source noteuspto-grants-2006_07