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Sodium borohydride → 2-(4-(Hydroxymethyl)-1H-indol-1-yl)benzonitrile

HRID 1055402
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반응식

HRID 1055402 반응식
[BH4-].[Na+].[CH:3]([C:5]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:6]=1[CH:7]=[CH:8][N:9]2[C:14]1[CH:21]=[CH:20][CH:19]=[CH:18][C:15]=1[C:16]#[N:17])=[O:4]>CCO.C(Cl)Cl>[OH:4][CH2:3][C:5]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:6]=1[CH:7]=[CH:8][N:9]2[C:14]1[CH:21]=[CH:20][CH:19]=[CH:18][C:15]=1[C:16]#[N:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 4311764Sodium borohydrideHCID 900374192-(4-formyl-1H-indol-1-yl)benzonitrile

생성물 1

HCID 189504042-(4-(Hydroxymethyl)-1H-indol-1-yl)benzonitrile수율 99.2%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 6344Dichloromethane용매

실험 절차

NaBH4 (50 mg, 1.35 mmol Eq: 0.4) was added to a solution of 2-(4-formyl-1H-indol-1-yl)benzonitrile (810 mg, 3.29 mmol, Eq: 1.00) in EtOH (30 mL) and DCM (15 mL) at 0° C. and the mixture warmed to RT. After 3 h., the mixture was concentrated to remove the DCM. The resulting mixture was diluted with sat. NH4Cl, extracted with DCM and the combined extracts concentrated. The residue was purified by silica gel chromatography to afford the title compound (810 mg, 99%) as a white solid.

후처리

  1. concentrationthe mixture was concentrated
  2. customto remove the DCM
  3. additionThe resulting mixture was diluted with sat. NH4Cl
  4. extractionextracted with DCM
  5. concentrationthe combined extracts concentrated
  6. customThe residue was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-74518f6644234fe796b3a4c9b7f9c9fb
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394263B2

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