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

HRID 1512739
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HRID 1512739 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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+)

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후처리

  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

출처 및 근거

ORD 기록
ord-8b4022c50aac4f278f6a4019191ae3e8
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08217028B2

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