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Benzyl Bromide → (2S,5R)-1-Benzyl-2,5-dimethylpiperazine

HRID 457737
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인쇄 미리보기

반응식

HRID 457737 반응식
[CH3:1][C@H:2]1[CH2:7][NH:6][C@H:5]([CH3:8])[CH2:4][NH:3]1.[CH2:9](Br)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>C(O)C>[CH2:9]([N:3]1[CH2:4][C@@H:5]([CH3:8])[NH:6][CH2:7][C@@H:2]1[CH3:1])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7498Benzyl BromideHCID 2206722,5-Dimethylpiperazine, trans-

생성물 1

HCID 23402345(2S,5R)-1-Benzyl-2,5-dimethylpiperazine

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

50 g trans-2,5 dimethylpiperazine was dissolved in 300 mL ethanol and treated with 26.36 mL (½ equivalents) benzylbromide. The mixture was stirred at room temperature for 12 hours and concentrated. The residue was taken up in ethyl acetate and washed with 10% aqueous sodium bicarbonate and saturated sodium chloride; dried over anhydrous magnesium sulfate and concentrated to give crude 1-benzyl-trans-2,5-dimethylpiperazine, as an oil.

후처리

  1. concentrationconcentrated
  2. washwashed with 10% aqueous sodium bicarbonate and saturated sodium chloride
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ec0de4f6d6c3494487621aebb6e6824c
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07189726B2

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