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Methanol → 2-(hydroxymethyl)-1H-indole-5-carbonitrile

HRID 1512739
ノート
印刷プレビュー

反応式

HRID 1512739 の反応式
[H-].[H-].[H-].[H-].[Li+].[Al+3].[C:7]([C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][C:13]([C:18](OCC)=[O:19])=[CH:12]2)#[N:8].CO>C1COCC1>[OH:19][CH2:18][C:13]1[NH:14][C:15]2[C:11]([CH:12]=1)=[CH:10][C:9]([C:7]#[N:8])=[CH:17][CH:16]=2
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 887MethanolHCID 4714953Ethyl 5-cyanoindole-2-carboxylateHCID 21226445Aluminium lithium hydride

生成物 1

HCID 135679562-(hydroxymethyl)-1H-indole-5-carbonitrile収率 74.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

LiAlH4 (1.0 M in THF, 5 mL) was added to a solution of ethyl 5-cyano-1H-indole-2-carboxylate (D21) (1 g) in THF (100 mL). The reaction mixture was stirred for 15 min at RT. MeOH was added to quench the reaction. The solvent was evaporated. EtOAc (500 mL) was added. The organic solution was washed with aqueous HCl (300 mL), then was dried over anhydrous magnesium sulfate. The dried solution was concentrated to afford 2-(hydroxymethyl)-1H-indole-5-carbonitrile (D24) (600 mg) as a pale orange oil. MS (ES): C10H8N2O requires 172; found 173.2 (M+H+)

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customto quench
  2. customthe reaction
  3. customThe solvent was evaporated
  4. additionEtOAc (500 mL) was added
  5. washThe organic solution was washed with aqueous HCl (300 mL)
  6. dry with materialwas dried over anhydrous magnesium sulfate
  7. concentrationThe dried solution was concentrated

出典と根拠

ORDレコード
ord-8b4022c50aac4f278f6a4019191ae3e8
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08217028B2

反応ノート

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