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Tetrahydrofuran → 6-Methoxy-5-methyl-1H-indole

HRID 73340
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HRID 73340 반응식
[CH3:1][O:2][C:3]1[C:8]([CH3:9])=[CH:7][C:6]([CH2:10][C:11]#N)=[C:5]([N+:13]([O-])=O)[CH:4]=1.O1CCCC1>[C].[Pd].C(O)CCC>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:6]([CH:10]=[CH:11][NH:13]2)=[CH:7][C:8]=1[CH3:9]
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참가 물질

5

반응물 2

HCID 8028TetrahydrofuranHCID 58437287(4-Methoxy-5-methyl-2-nitrophenyl)acetonitrile

생성물 1

HCID 198038376-Methoxy-5-methyl-1H-indole수율 69.3%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 2631-Butanol용매

반응 조건

온도
60 °C

실험 절차

To a solution of (4-methoxy-5-methyl-2-nitrophenyl)acetonitrile (0.24 g) in a mixed solvent of tetrahydrofuran (2 mL) and n-butanol (2 mL) was added palladium-carbon powder (0.043 g) under an argon atmosphere and this mixture was stirred at 60° C. under a hydrogen atmosphere for 36 hours. The insoluble material was removed by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate) to give the title compound (0.13 g).

후처리

  1. customThe insoluble material was removed by filtration
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customThe residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-b2862c0f5dcd4d04acb2d1ace9e19f83
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08829040B2

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