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Butanal → N,N-Di(propan-2-yl)but-1-en-1-amine

HRID 856840
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인쇄 미리보기

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HRID 856840 반응식
[CH:1](=O)[CH2:2][CH2:3][CH3:4].[CH:6]([NH:9][CH:10]([CH3:12])[CH3:11])([CH3:8])[CH3:7]>C1C=CC=CC=1>[CH:6]([N:9]([CH:1]=[CH:2][CH2:3][CH3:4])[CH:10]([CH3:12])[CH3:11])([CH3:8])[CH3:7]
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참가 물질

4

반응물 2

HCID 261ButanalHCID 7912Diisopropylamine

생성물 1

HCID 53723651N,N-Di(propan-2-yl)but-1-en-1-amine수율 65%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

6.25 ml (69.3 mmol) of butyraldehyde and 19.44 ml (139 mmol) of diisopropylamine were dissolved in 30 ml of benzene, and the mixture was heated under reflux, while removing the water produced, until the production of water stopped (about 15 hours). The solvent was then removed by distillation under reduced pressure, and the residue was distilled under atmospheric pressure. Those fractions of the distillate having a boiling point of from 140 to 160° C. were collected, to give 6.95 g of the title compound as a pale yellow oily substance (yield 65%).

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux
  3. customwhile removing the water
  4. customproduced, until the production of water
  5. custom(about 15 hours)
  6. customThe solvent was then removed by distillation under reduced pressure
  7. distillationthe residue was distilled under atmospheric pressure
  8. customof from 140 to 160° C.
  9. customwere collected

출처 및 근거

ORD 기록
ord-b1f4b954edb34e5c9a6451808d73c45e
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE039420E1

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