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Diisobutylaluminum hydride → (3-iodo-1-methyl-1H-indazol-5-yl)methanol

HRID 246338
ノート
印刷プレビュー

反応式

HRID 246338 の反応式
C[O:2][C:3]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH3:14])[N:9]=[C:8]2[I:15])=O.CC(C[AlH]CC(C)C)C>C(Cl)Cl>[I:15][C:8]1[C:7]2[C:11](=[CH:12][CH:13]=[C:5]([CH2:3][OH:2])[CH:6]=2)[N:10]([CH3:14])[N:9]=1
参加物反応条件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 14487Diisobutylaluminum hydrideHCID 71279594Methyl 3-iodo-1-methyl-1H-indazole-5-carboxylate

生成物 1

HCID 71280092(3-iodo-1-methyl-1H-indazol-5-yl)methanol収率 93.4%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

To a solution of 3-iodo-1-methyl-1H-indazole-5-carboxylic acid methyl ester (0.95 g, 3.01 mmol) in CH2Cl2 (30 mL) at 0° C. was slowly added DIBAL-H (1.18 mL, 6.61 mmol). The reaction mixture was stirred at 0° C. for 1.5 h. Carefully quenched with MeOH (1 mL) then diluted with CH2Cl2 (20 mL) and added saturated aqueous Na+K+ tartrate (30 mL). The biphasic mixture was stirred vigorously at room temp for 1 h. The layers were separated and the aqueous phase was extracted with CH2Cl2. The combined organics were washed with water then dried over MgSO4 and concentrated to afford 810 mg of (3-iodo-1-methyl-1H-indazol-5-yl)methanol as a yellow waxy solid.

後処理

  1. customat 0° C.
  2. customCarefully quenched with MeOH (1 mL)
  3. additionthen diluted with CH2Cl2 (20 mL)
  4. additionadded saturated aqueous Na+K+ tartrate (30 mL)
  5. stirringThe biphasic mixture was stirred vigorously at room temp for 1 h
  6. customThe layers were separated
  7. extractionthe aqueous phase was extracted with CH2Cl2
  8. washThe combined organics were washed with water
  9. dry with materialthen dried over MgSO4
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-2bc6f15d51aa4840af5cc95f4a7e8df8
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658646B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート