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HRID 447472作成日:2026年10月25日

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

https://huagongshe.com/reaction/447472

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物CyclopentanoneHCID 8452—
反応物1-(4-Iodophenyl)piperazineHCID 4147845—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒Dce thfHCID 21493386—
生成物1-Cyclopentyl-4-(4-iodophenyl)piperazineHCID 5848626182%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481525B2
出典データセットuspto-grants-2013_07
ORD IDord-4d07a7d3b0134e96aa86221594b6a80e
出典メモuspto-grants-2013_07