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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 447474생성일: 2026년 10월 24일

Acetic Acid → 1-(4-Iodophenyl)-4-isopropylpiperazine

https://huagongshe.com/ko/reaction/447474

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물AcetoneHCID 180—
반응물1-(4-Iodophenyl)piperazineHCID 4147845—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매Dce thfHCID 21493386—
생성물1-(4-Iodophenyl)-4-isopropylpiperazineHCID 5848618985%

반응 단계

To a mixture of 1-(4-iodophenyl)piperazine (1.44 g, 5 mmol) and acetone (1.47 mL, 20 mmol) in DCE/THF (45 mL/15 mL) was added NaBH(OAc)3 (1.38 g, 6.5 mmol), followed by AcOH (0.5 mL). After addition, the resulting mixture was stirred O/N at rt. The reaction as quenched with sat. NaHCO3 (10 mL) and H2O (20 mL), and was then extracted with EtOAc (2×60 mL), dried over MgSO4 and concentrated to give the crude title compound as a light yellow solid (1.396 g, 85%). 1H NMR (400 MHz, DMSO-d6) δ 7.46 (d, J=8.4 Hz, 2H), 6.75 (d, J=8.8 Hz, 2H), 3.12-3.07 (m, 4H), 2.65 (p, J=6.5 Hz, 1H), 2.56-2.52 (m, 4H), 0.98 (d, J=6.4 Hz, 6H); MS ESI 330.9 [M+H]+, calcd. for [C13H19IN2+H]+ 331.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481525B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-6a5604dba86145ba82ee56d088d41765
출처 메모uspto-grants-2013_07