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Sodium borohydride → 2-Hydroxymethyl-1-methyl-4-phenyl-5-(4-pyridyl)imidazole

HRID 1387644
ノート
印刷プレビュー

反応式

HRID 1387644 の反応式
[CH:1]([C:3]1[N:4]([CH3:20])[C:5]([C:14]2[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=2)=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[N:7]=1)=[O:2].[BH4-].[Na+]>CO>[OH:2][CH2:1][C:3]1[N:4]([CH3:20])[C:5]([C:14]2[CH:15]=[CH:16][N:17]=[CH:18][CH:19]=2)=[C:6]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[N:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 4311764Sodium borohydrideHCID 187715342-Formyl-1-methyl-4-phenyl-5-[4-pyridyl]imidazole

生成物 1

HCID 187715292-Hydroxymethyl-1-methyl-4-phenyl-5-(4-pyridyl)imidazole

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 2-formyl-1-methyl-4-phenyl-5-[4-pyridyl]imidazole (0.830 g, 3.15 mmol) in MeOH at 0° C. was added NaBH4 (0.143 g, 3.78 mmol). The mixture was stirred at rt for 0.5 h when the solvent was evaporated in vacuo and the residue was partitioned between CH2Cl2 and H2O. The organic extract was washed with aqueous NaCl and dried (MgSO4). The solvent was removed in vacuo and the residue was purified by flash chromatography eluting with 25:1 CH2Cl2/MeOH. The title compound was obtained as a white solid (0.608 g, 73%): mp 236-238° C.

後処理

  1. customwas evaporated in vacuo
  2. customthe residue was partitioned between CH2Cl2 and H2O
  3. extractionThe organic extract
  4. washwas washed with aqueous NaCl
  5. dry with materialdried (MgSO4)
  6. customThe solvent was removed in vacuo
  7. customthe residue was purified by flash chromatography
  8. washeluting with 25:1 CH2Cl2/MeOH

出典と根拠

ORDレコード
ord-363d3869861a4194af920e4fe3cd6bdd
出典データセット
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06268370B1

反応ノート

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