HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792986Generated: October 25, 2026
Triphenylphosphine → HCID 22024880, compound
https://huagongshe.com/reaction/1792986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 1-(4-Fluorophenyl)-2-(piperazin-1-yl)ethan-1-one | HCID 16769083 | — |
| Reactant | 4-Hydroxymethyl-2,6-bis-pentyloxyphenol | HCID 22024906 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22024880 | HCID 22024880 | 15.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07078407B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-775e1765b7fa43c09871eef7ae04f3c2 |
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| Source note | uspto-grants-2006_07 |
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