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Ammonium Chloride → [4-(2-Methylimidazol-1-yl)phenyl]methanol

HRID 1291045
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HRID 1291045 반응식
[CH3:1][C:2]1[N:3]([C:7]2[CH:14]=[CH:13][C:10]([CH:11]=[O:12])=[CH:9][CH:8]=2)[CH:4]=[CH:5][N:6]=1.[BH4-].[Na+].[NH4+].[Cl-]>CO>[CH3:1][C:2]1[N:3]([C:7]2[CH:14]=[CH:13][C:10]([CH2:11][OH:12])=[CH:9][CH:8]=2)[CH:4]=[CH:5][N:6]=1
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참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 31596624-(2-Methyl-1H-imidazol-1-yl)benzaldehydeHCID 4311764Sodium borohydride

생성물 1

HCID 11735617[4-(2-Methylimidazol-1-yl)phenyl]methanol수율 50.5%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a stirred solution of the crude 4-(2-methylimidazol-1-yl)benzaldehyde (1.0 g) in methanol(15 ml) cooled to 0° C. was added NaBH4 (0.2 g, 5.2 mmol) in portions over 15 min and the whole stirred for 1 h. A saturated aqueous NH4Cl solution (50 ml) was added to the reaction mixture and the whole extracted with ethyl acetate (100 ml×2). The organic layer was washed with water (100 ml), brine (50 ml), dried over MgSO4, and solvent removed under reduced pressure. The crude product was washed with an Et2O/ethyl acetate mixture (3:1, 15 ml) to give the title compound (0.51 g, 50 %) as a white powder. 1H NMR (CDCl3) δ: 7.5 (d, 2H, J=8 Hz), 7.28 (d, 2H, J=8 Hz), 7.01 (d, 1H, J=1 Hz), 6.99 (d, 1H, J=1 Hz), 4.78 (s, 2H), 2.35 (s, 3H).

후처리

  1. extractionthe whole extracted with ethyl acetate (100 ml×2)
  2. washThe organic layer was washed with water (100 ml), brine (50 ml)
  3. dry with materialdried over MgSO4, and solvent
  4. customremoved under reduced pressure
  5. washThe crude product was washed with an Et2O/ethyl acetate mixture (3:1, 15 ml)

출처 및 근거

ORD 기록
ord-bc71e60e4a684e24aa7197a8d701537d
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05753682

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