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2-(2-Methyl-1-buten-4-yl)indole → Isopentylindol

HRID 1956546
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반응식

HRID 1956546 반응식
[CH3:1][C:2]([CH2:4][CH2:5][C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH2:3]>[Pd].C(O)C>[CH3:1][CH:2]([CH3:3])[CH2:4][CH2:5][C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 187616282-(2-Methyl-1-buten-4-yl)indole

생성물 1

HCID 11041488Isopentylindol수율 59%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

Into a 3-necked round bottom flask under a blanket of nitrogen was placed 5% palladium catalyst on charcoal (771 mg). A solution of 2-(2-methyl-1-buten-4-yl) indole (671 mg) in ethanol (36 ml) was added to the flask, which was evacuated and charged with hydrogen twice. The mixture was stirred vigorously under hydrogen (1 atm) for 2 h, followed by filtration through a pad of Celite. The solvent was removed under reduced pressure and the crude residue was purified by flash chromatography (3% ethyl acetate/hexane) to give 2-(3-methyl-n-butyl) indole (400 mg, 59%) as a yellow crystalline solid.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customInto a 3-necked round bottom flask under a blanket of nitrogen was placed
  2. customwas evacuated
  3. additioncharged with hydrogen twice
  4. filtrationfollowed by filtration through a pad of Celite
  5. customThe solvent was removed under reduced pressure
  6. customthe crude residue was purified by flash chromatography (3% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-2d3c9739290f4f22a3133242abc82c7d
출처 데이터셋
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05780496

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