HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447472Generated: October 25, 2026
Acetic Acid → 1-Cyclopentyl-4-(4-iodophenyl)piperazine
https://huagongshe.com/reaction/447472
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | 1-(4-Iodophenyl)piperazine | HCID 4147845 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Dce thf | HCID 21493386 | — |
| Product | 1-Cyclopentyl-4-(4-iodophenyl)piperazine | HCID 58486261 | 82% |
Reaction Steps
To a mixture of 1-(4-iodophenyl)piperazine (1.44 g, 5 mmol) and cyclopentanone (840 mg, 10 mmol) in DCE/THF (40 mL/20 mL) was added NaBH(OAc)3 (1.484 g, 7 mmol), followed by AcOH (0.5 mL). After addition, the resulting mixture was stirred 22 h at rt. After quenching with sat. NaHCO3 (20 mL), H2O (20 mL) and brine (20 mL), the solution was extracted with EtOAc (60 mL+30 mL). Removal of solvents, followed by trituration with MeOH afforded the crude title compound as a pale yellow solid (1.46 g, 82%). 1H NMR (400 MHz, DMSO-d6) δ 7.52 (d, J=8.4 Hz, 2H), 6.70 (d, J=8.4 Hz, 2H), 3.20 (t, J=4.8 Hz, 4H), 2.66 (t, J=4.6 Hz, 4H), 2.54 (p, J=7.6 Hz, 1H), 1.96-1.87 (m, 2H), 1.78-1.52 (m, 4H), 1.50-1.38 (m, 2H); MS ESI 357.0 [M+H]+, calcd. for [C15H21N2+H]+ 357.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481525B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-4d07a7d3b0134e96aa86221594b6a80e |
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| Source note | uspto-grants-2013_07 |
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