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4-(2-(Tetrahydropyran-2-yloxy)ethyl)-1-(2-azidoethyl)benzene → 4-(2-(Tetrahydropyran-2-yloxy)ethyl)phenethylamine

HRID 1756018
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반응식

HRID 1756018 반응식
[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][CH2:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][CH2:17][N:18]=[N+]=[N-])=[CH:12][CH:11]=1>C(O)C.[C].[Pd]>[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][CH2:9][C:10]1[CH:11]=[CH:12][C:13]([CH2:16][CH2:17][NH2:18])=[CH:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 224076064-(2-(Tetrahydropyran-2-yloxy)ethyl)-1-(2-azidoethyl)benzene

생성물 1

HCID 224076104-(2-(Tetrahydropyran-2-yloxy)ethyl)phenethylamine수율 72%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매

실험 절차

To a solution of 4-(2-(tetrahydropyran-2-yloxy)ethyl)-1-(2-azidoethyl)benzene (4.30 g, 15.61 mmol) in ethanol was added 10% palladium-carbon (0.10 g). The mixture was stirred under an atmosphere of hydrogen gas at room temperature for 16 hours. Then 10% palladium-carbon was filtered off, and the solvent was evaporated. The residue was purified by column chromatography on silica gel eluting with ethyl acetate/methanol (=8/2) to give the desired 4-(2-(tetrahydropyran-2-yloxy)ethyl)phenethylamine (2.80 g, 72%).

후처리

  1. filtrationThen 10% palladium-carbon was filtered off
  2. customthe solvent was evaporated
  3. customThe residue was purified by column chromatography on silica gel eluting with ethyl acetate/methanol (=8/2)

출처 및 근거

ORD 기록
ord-5daffc88081b4f59bd00d29dd700af0a
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05439911

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