돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1350395생성일: 2026년 10월 27일

Dichloromethane → (S)-1-Benzyl-3-(3-phenyl-allyl)-piperazine

https://huagongshe.com/reaction/1350395

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Trifluoroacetic acidHCID 6422—
반응물Sodium HydroxideHCID 14798—
반응물(S)-4-Benzyl-2-(3-phenyl-allyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 69486789—
용매TolueneHCID 1140—
생성물(S)-1-Benzyl-3-(3-phenyl-allyl)-piperazineHCID 6948696782.7%

반응 단계

Dissolve (S)-4-benzyl-2-(3-phenyl-allyl)-piperazine-1-carboxylic acid tert-butyl ester (2.37 g, 6.04 mmol) in toluene (50 mL) and treat with trifluoroacetic acid (10.3 g, 90.5 mmol) at room temperature, and stir the reaction mixture. After overnight, dilute the reaction with CH2Cl2, and basify with 2N NaOH (50 mL), extract the aqueous solution with CH2Cl2, wash the combined organic layers brine, dry over Na2SO4. Pass the crude product through a SCX column (10 g), collect the 0.2N NH3/MeOH eluent and concentrate to give 1.46 g of the title compound: mass spectrum (Electrospray): m/z=293.3 (M+1). 1H NMR (400 MHz, CDCl3): δ7.35–7.19 (m, 10H), 6.54–6.47 (m, 1H) 6.18–6.11, 5.70–5.60 (m, 1H), 3.70 (s, 2H), 2.97–2.73 (m, 5H), 2.40–2.18 (m, 2H), 2.09–2.00 (m, 1H), 1.83 (t, 1H, J=9.8 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07214673B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-add402295cd54915982ffe69bcffa438
출처 메모uspto-grants-2007_05