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4-Bromobenzyl bromide → 1-(4-Bromobenzyl)piperidin-4-ol

HRID 1291132
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HRID 1291132 반응식
[OH:1][CH:2]1[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.[Br:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13]Br)=[CH:11][CH:10]=1>CN(C)C=O>[Br:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13][N:5]2[CH2:6][CH2:7][CH:2]([OH:1])[CH2:3][CH2:4]2)=[CH:11][CH:10]=1
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참가 물질

4

반응물 2

HCID 685274-Bromobenzyl bromideHCID 79341Piperidin-4-ol

생성물 1

HCID 6777721-(4-Bromobenzyl)piperidin-4-ol수율 100%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

0.202 g (0.002 mol) of 4-hydroxypiperidine and 0.55 g (0.0022 mol) of 4-bromobenzyl bromide were dissolved in 5 ml of dimethylformamide and stirred at room temperature for 2 hrs. The solvent was distilled off and the residue was taken up in dichloromethane and washed with sat. bicarbonate solution and sodium chloride solution. The organic phase was dried over sodium sulfate and concentrated. 0.54 g (100%) of 1-(4-bromo-benzyl)-piperidin-4-ol was obtained as a colorless oil. MS: me/e (% basic peak)=271, 269 (C12H16BrNO30 , 73, 76), 270, 268 (79, 70), 171, 169 (99, 100), 114 (64), 100 (60).

후처리

  1. distillationThe solvent was distilled off
  2. washwashed with sat. bicarbonate solution and sodium chloride solution
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-b0cce427147d4cf58f2bbf443e200515
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05753679

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