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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281739Generated: October 25, 2026

Acetic Acid → 1-Cyclopentyl-4-(4-iodophenyl)piperazine

https://huagongshe.com/reaction/2281739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclopentanoneHCID 8452—
Reactant1-(4-Iodophenyl)piperazineHCID 4147845—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDce thfHCID 21493386—
Product1-Cyclopentyl-4-(4-iodophenyl)piperazineHCID 5848626182%

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 [C15H21IN2+H]+ 357.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139563B2
Source datasetuspto-grants-2015_09
ORD IDord-f1728bf424bf4cf6908ce32f3bc202d1
Source noteuspto-grants-2015_09