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2-(1-Cyclohexenyl)ethylamine → [2-(Cyclohex-1-en-1-yl)ethyl](methyl)amine

HRID 383133
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HRID 383133 반응식
[C:1]1([CH2:7][CH2:8][NH2:9])[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1.[C:10](OC(OC(OC(C)(C)C)=O)=O)(C)(C)C>O1CCOCC1>[CH3:10][NH:9][CH2:8][CH2:7][C:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 769382-(1-Cyclohexenyl)ethylamineHCID 90495Di-tert-butyl dicarbonate

생성물 1

HCID 18360934[2-(Cyclohex-1-en-1-yl)ethyl](methyl)amine수율 18%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

To a solution of 2-(1-cyclohexenyl)ethylamine (4.0 g) in 1,4-dioxane (40 mL) was added di-tert-butyldicarbonate (7.7 g). After gas evolution ceased (≈2 h) the reaction was concentrated. A portion of the residue (2 g) was dissolved in THF (10 mL) followed by addition of LiAlH4 (10 mL, 1M THF), which caused an exotherm. After 3 h, more LiAlH4 solution was added (4 mL), and the reaction was warmed to reflux. After 1 h, the reaction was cooled, and quenched cautiously with vigorous stirring by the addition of water (0.57 mL), 1M NaOH (0.6 mL), and more water (1.5 mL). The suspension was filtered through celite, which was washed with ether. The organic solution was concentrated to give the desired product as a volatile oil (0.8 g).

후처리

  1. custom(≈2 h)
  2. concentrationwas concentrated
  3. dissolutionA portion of the residue (2 g) was dissolved in THF (10 mL)
  4. additionfollowed by addition of LiAlH4 (10 mL, 1M THF), which
  5. additionmore LiAlH4 solution was added (4 mL)
  6. temperaturethe reaction was warmed to reflux
  7. waitAfter 1 h
  8. temperaturethe reaction was cooled
  9. customquenched cautiously
  10. filtrationThe suspension was filtered through celite, which
  11. washwas washed with ether
  12. concentrationThe organic solution was concentrated

출처 및 근거

ORD 기록
ord-7f058490acaa40edb293e6929fcdbcd0
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06310095B1

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