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1-Methyl-1,4-cyclohexadiene → HCID 86722311, 화합물

HRID 874820
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HRID 874820 반응식
[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[CH2:6][CH2:7][N:8](CC1C=CC=CC=1)[CH2:9][CH2:10][O:11][Si:12]([C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:14])[CH3:13].CC1CC=CCC=1>C(O)C.[Pd]>[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[CH2:6][CH2:7][NH:8][CH2:9][CH2:10][O:11][Si:12]([C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:14])[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 780061-Methyl-1,4-cyclohexadieneHCID 86722309HCID 86722309, 화합물

생성물 1

HCID 86722311HCID 86722311, 화합물수율 91%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a stirred solution of N-(2-(1,3-dioxolan-2-yl)ethyl)-N-benzyl-2-((tert-butyldimethylsilyl)oxy)ethanamine (3.87 g, 10.6 mmol) in ethanol (100 mL) was added 10% palladium on carbon (1.93 g) and 1-methyl-1,4-cyclohexadiene (5.93 mL, 53.0 mmol). The suspension was heated at reflux for 30 minutes and allowed to cool. The suspension was filtered through celite and the filter cake washed with further ethanol. The solvent was evaporated at reduced pressure to afford the title compound (2.64 g, 91%).

후처리

  1. temperatureThe suspension was heated
  2. temperatureat reflux for 30 minutes
  3. temperatureto cool
  4. filtrationThe suspension was filtered through celite
  5. washthe filter cake washed with further ethanol
  6. customThe solvent was evaporated at reduced pressure

출처 및 근거

ORD 기록
ord-c411ac4acbf94616b507fb77c7f65ae3
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08980913B2

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