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Acetic Acid → 4-Amino-3-[(1-benzyl-piperidin-4-yl-amino)-methyl]phenol

HRID 2355939
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HRID 2355939 반응식
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([NH:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[N+:22]([O-])=O)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(O)(=[O:27])C>[Zn]>[NH2:22][C:17]1[CH:18]=[CH:19][C:20]([OH:27])=[CH:21][C:16]=1[CH2:15][NH:14][CH:11]1[CH2:12][CH2:13][N:8]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH2:9][CH2:10]1
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참가 물질

4

반응물 2

HCID 176Acetic AcidHCID 48487621-benzyl-N-[(2-nitrophenyl)methyl]piperidin-4-amine

생성물 1

HCID 588643124-Amino-3-[(1-benzyl-piperidin-4-yl-amino)-methyl]phenol수율 79%

시약·촉매·용매 1

HCID 23994Zinc촉매

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온도
60 °C

실험 절차

(1-Benzyl-piperidin-4-yl)-(2-nitro-benzyl)-amine (0.25 g, 0.7 mmol) and zinc dust (0.2 g, excess) were combined in 75% aqueous acetic acid (8 mL) and stirred at 60° C. for 2 h. After cooling to room temperature, the solvents were removed in vacuo and the resultant crude mixture dissolved in water (10 mL), followed by addition of ammonium hydroxide until pH 3 was attained. The solution was extracted with methylene chloride (3×). The organic layers were pooled together, washed with water (2×), brine (2×), dried over sodium sulfate, filtered, and concentrated to afford 0.18 g (79%) of the desired product.

후처리

  1. temperatureAfter cooling to room temperature
  2. customthe solvents were removed in vacuo
  3. dissolutionthe resultant crude mixture dissolved in water (10 mL)
  4. additionfollowed by addition of ammonium hydroxide until pH 3
  5. extractionThe solution was extracted with methylene chloride (3×)
  6. washwashed with water (2×), brine (2×)
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0e0975ede537443ebfc1fc8931942f3f
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07754732B2

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