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Benzylethanolamine → 4-Benzyl-2-(methoxymethyl)morpholine

HRID 373915
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HRID 373915 반응식
[CH2:1]([NH:8][CH2:9][CH2:10]O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[O:12]1[CH:14]([CH2:15][O:16][CH3:17])[CH2:13]1>>[CH2:1]([N:8]1[CH2:9][CH2:10][O:12][CH:14]([CH2:15][O:16][CH3:17])[CH2:13]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

3

반응물 2

HCID 4348BenzylethanolamineHCID 135891,2-Epoxy-3-methoxypropane

생성물 1

HCID 103534614-Benzyl-2-(methoxymethyl)morpholine수율 58.2%

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온도
50 °C

실험 절차

N-Benzylethanolamine (459 g) is mixed with 1,2-epoxy-3-methoxypropane (422 g) and the mixture is stirred at 50° C. for 16 hours and thereafter the excess 1,2-epoxy-3-methoxypropane is distilled off under reduced pressure. The residue is dissolved in 1,4-dioxane (3 liters) and thereto are added powdery potassium hydroxide (692.5 g) and tris(3,6-dioxaheptyl)amine (11.4 g). To the mixture is added dropwise with stirring a solution of p-toluenesulfonyl chloride (809.4 g) in 1,4-dioxane (2 liters) over a period of 1.5 hour, during which the temperature of the reaction mixture raises and the solvent is refluxed. After the dropwise addition, the mixture is stirred for 2 hours, and the undissolved materials are filtered off and washed with ethyl acetate. The filtrate and the washing liquid are combined and distilled under reduced pressure to remove the solvent. To the residue are added water (600 ml) and conc. hydrochloric acid (300 ml) to make acidic. The aqueous layer is washed with ethyl acetate, made strongly basic by adding sodium hydroxide (160 g) under ice cooling and extracted with ethyl acetate. The ethyl acetate layer is washed with saturated saline solution, dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent. The obtained residue is distilled under reduced pressure to give the title compound (391.3 g) as colorless liquid.

후처리

  1. distillationthe excess 1,2-epoxy-3-methoxypropane is distilled off under reduced pressure
  2. dissolutionThe residue is dissolved in 1,4-dioxane (3 liters)
  3. additionare added powdery potassium hydroxide (692.5 g) and tris(3,6-dioxaheptyl)amine (11.4 g)
  4. additionTo the mixture is added dropwise
  5. stirringwith stirring a solution of p-toluenesulfonyl chloride (809.4 g) in 1,4-dioxane (2 liters) over a period of 1.5 hour
  6. temperatureduring which the temperature of the reaction mixture raises
  7. temperaturethe solvent is refluxed
  8. additionAfter the dropwise addition
  9. stirringthe mixture is stirred for 2 hours
  10. filtrationthe undissolved materials are filtered off
  11. washwashed with ethyl acetate
  12. distillationdistilled under reduced pressure
  13. customto remove the solvent
  14. additionTo the residue are added water (600 ml) and conc. hydrochloric acid (300 ml)
  15. washThe aqueous layer is washed with ethyl acetate
  16. additionby adding sodium hydroxide (160 g) under ice cooling
  17. extractionextracted with ethyl acetate
  18. washThe ethyl acetate layer is washed with saturated saline solution
  19. dry with materialdried over anhydrous magnesium sulfate
  20. distillationdistilled under reduced pressure
  21. customto remove the solvent
  22. distillationThe obtained residue is distilled under reduced pressure

출처 및 근거

ORD 기록
ord-8f6f26ee04f54e2989fb11d1fe584eeb
출처 데이터셋
uspto-grants-1992_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05166203

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