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5-Benzyloxy-1-heptylindole → HCID 68839366, 화합물

HRID 1821961
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반응식

HRID 1821961 반응식
C([O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[N:14]([CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH:13]=[CH:12]2)C1C=CC=CC=1>CO.ClCCl.[Pd]>[CH2:18]([N:14]1[C:15]2[C:11](=[CH:10][C:9]([OH:8])=[CH:17][CH:16]=2)[CH:12]=[CH:13]1)[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 688426665-Benzyloxy-1-heptylindole

생성물 1

HCID 68839366HCID 68839366, 화합물

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 6344Dichloromethane용매

실험 절차

0.5 g (1.55 mmol) 5-benzyloxy-1-heptylindole is dissolved in a Schlenk flask in 10 ml methanol and 4 ml dichloromethane. 0.06 g Pd (10%)/C is added and the mixture is rinsed with nitrogen for 15 minutes. Thereafter, a balloon filled with hydrogen is placed on the Schlenk piston and hydrogenation is carried out at room temperature for 12 h. The batch is filtrated on a frit and the solvent is removed in vacuo. The residue is purified on silica gel by means of column chromatography (flow agent: hexane/ethyl acetate 9:1). The product accrues as an oil.

후처리

  1. washthe mixture is rinsed with nitrogen for 15 minutes
  2. additionThereafter, a balloon filled with hydrogen
  3. filtrationThe batch is filtrated on a frit
  4. customthe solvent is removed in vacuo
  5. customThe residue is purified on silica gel by means of column chromatography (flow agent: hexane/ethyl acetate 9:1)

출처 및 근거

ORD 기록
ord-ec2be7085d344be6ad50bab997d434e9
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07608633B2

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