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Ethanol → [4-(2-Morpholinoethoxy)phenyl]methylamine

HRID 1456034
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HRID 1456034 반응식
[N:1]1([CH2:7][CH2:8][O:9][C:10]2[CH:17]=[CH:16][C:13]([C:14]#[N:15])=[CH:12][CH:11]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.C(O)C>Cl.O=[Pt]=O.C(Cl)(Cl)Cl>[N:1]1([CH2:7][CH2:8][O:9][C:10]2[CH:17]=[CH:16][C:13]([CH2:14][NH2:15])=[CH:12][CH:11]=2)[CH2:2][CH2:3][O:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 702EthanolHCID 29940744-(2-Morpholin-4-ylethoxy)benzonitrile

생성물 1

HCID 7164631[4-(2-Morpholinoethoxy)phenyl]methylamine수율 79.3%

시약·촉매·용매 3

HCID 313Hydrochloric Acid촉매HCID 345198Adams' catalyst촉매HCID 6212Chloroform용매

실험 절차

A mixture of 4-[2-(4-morpholinyl)ethoxy]benzonitrile (0.93 g, 4 mmol), ethanol (100 mL), CHCl3 (4 mL) and PtO2 (100 mg) was hydrogenated at 45 psi on a Parr hydrogenator for 8 hours. Concentrated HCl (2-3 drops) was then added to the reaction mixture and the hydrogenation was continued for another 10 hours. The catalyst was removed by filtration, the filter cake was washed with ethanol and then the filtrate was evaporated to dryness. The residue was dissolved in water and then was saturated with solid K2CO3. The mixture was extracted with CH2Cl2 and then the CH2Cl2 layer was dried over K2CO3 and evaporated to afford 0.75 g (79%) of 4-[2-(4-morpholinyl)ethoxy]phenylmethylamine.

후처리

  1. waitthe hydrogenation was continued for another 10 hours
  2. customThe catalyst was removed by filtration
  3. washthe filter cake was washed with ethanol
  4. customthe filtrate was evaporated to dryness
  5. dissolutionThe residue was dissolved in water
  6. extractionThe mixture was extracted with CH2Cl2
  7. dry with materialthe CH2Cl2 layer was dried over K2CO3
  8. customevaporated

출처 및 근거

ORD 기록
ord-3911b1fbeed444aa9089d65edf470fdf
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05843956

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