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Ethanol → 2-(2-Aminoethoxy)naphthalene

HRID 518944
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HRID 518944 반응식
O.[OH-].[Ba+2].[OH-].C(O)C.[CH:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=[CH:10][C:9]=1[O:18][CH2:19][CH2:20][NH:21]C(=O)C>C(OCC)(=O)C>[CH:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=[CH:10][C:9]=1[O:18][CH2:19][CH2:20][NH2:21]
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참가 물질

6

반응물 4

HCID 702EthanolHCID 962Water2회HCID 4128976N-[2-(2-naphthyloxy)ethyl]acetamideHCID 6093286Barium hydroxide

생성물 1

HCID 27942452-(2-Aminoethoxy)naphthalene수율 103.2%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

반응 조건

온도
50 °C

실험 절차

A 3-neck round bottom flask was charged with water (50 mL) and barium hydroxide (12.27 g, 71.61 mmol) while stirring. The resulting slurry was charged with ethanol (50 mL) and finally N-(2-(naphthalen-2-yloxy)ethyl)acetamide (10.0 g, 35.80 mmol) as prepared above. The resulting mixture was heated to reflux for 18 h. The reaction was monitored by TLC. The reaction was then allowed to cool to 50° C., then charged with water (50 mL) followed by ethyl acetate (100 mL). The mixture was then stirred for 15 min. The mixture was then filtered and thelayers were separated. The upper organic layer was washed with saturated sodium chloride (50 mL) and dried over sodium sulfate and concentrate to afford 2-(2-naphthyloxy)ethylamine as an amber oil (6.92 g, 47%).

후처리

  1. customas prepared above
  2. temperatureThe resulting mixture was heated
  3. temperatureto reflux for 18 h
  4. stirringThe mixture was then stirred for 15 min
  5. filtrationThe mixture was then filtered
  6. customthelayers were separated
  7. washThe upper organic layer was washed with saturated sodium chloride (50 mL)
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrate

출처 및 근거

ORD 기록
ord-17d0ed3c05234243981bc0b3ddcb081e
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115237B2

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