HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447473Generated: October 30, 2026
Iodoethane → 1-Ethyl-4-(4-iodophenyl)piperazine
https://huagongshe.com/reaction/447473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(4-Iodophenyl)piperazine | HCID 4147845 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Ethyl-4-(4-iodophenyl)piperazine | HCID 13720669 | 85% |
Reaction Steps
To a stirred mixture of 1-(4-iodophenyl)piperazine (5.76 g, 20 mmol) and K2CO3 (5.44 g, 40 mmol) in acetone (200 mL) was added iodoethane (2.58 mL, 32 mmol) dropwise over 1 min. After addition, the resulting mixture was stirred at rt for 21 h. The resulting precipitate was filtered off and rinsed with EtOAc (2×60 mL). The filtrate was concentrated to dryness to give a whiteish yellow solid. Trituration with MeOH (10 mL) and H2O (250 mL), followed by suction filtration (rinsed with H2O) gave the title compound as a yellow solid (5.37 g, 85%) after drying. 1H NMR (400 MHz, DMSO-d6) δ 7.46 (d, J=7.6 Hz, 2H), 6.76 (d, J=8.0 Hz, 2H), 3.13-3.07 (m, 4H), 2.48-2.43 (m, 4H), 2.34 (q, J=7.2 Hz, 2H), 1.01 (t, J=7.2 Hz, 3H); MS ESI 317.0 [M+H]+, calcd. for [C12H17IN2+H]+ 317.0.
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-d1d8671cfc404a868d1a33d020029297 |
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| Source note | uspto-grants-2013_07 |
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