Hydrochloric Acid → 3-(Morpholin-4-yl)aniline

HRID 56122

Reaktionsgleichung

Reaktionsgleichung von HRID 56122
[O:1]1[CH2:6][CH2:5][N:4]([C:7]2[CH:8]=[C:9]([NH:13]C(=O)OC(C)(C)C)[CH:10]=[CH:11][CH:12]=2)[CH2:3][CH2:2]1.Cl>>[O:1]1[CH2:2][CH2:3][N:4]([C:7]2[CH:8]=[C:9]([CH:10]=[CH:11][CH:12]=2)[NH2:13])[CH2:5][CH2:6]1

Komponenten

3

Edukt 2

HCID 313Hydrochloric AcidHCID 101043125Tert-butyl (3-morpholinophenyl)carbamate

Produkt 1

HCID 8477683-(Morpholin-4-yl)anilineAusbeute 91 %

Versuchsvorschrift

A solution of tert-butyl (3-morpholinophenyl)carbamate (5.91 g, 21.20 mmol) in a solution of HCl (106 mL, 106.0 mmol, 1 M in MeOH) was stirred at rt overnight, then concentrated in vacuo. The residue was dissolved in water (100 mL). The soltution was basified with saturated Na2CO3 aqueous solution and extracted with CH2Cl2 (100 mL×3). The combined organic phases were washed with brine (150 mL), dried over anhydrous Na2SO4 and concentrated in vacuo to give the title compound as a light brown solid (3.42 g, 91%).

Aufarbeitung

  1. concentrationconcentrated in vacuo
  2. dissolutionThe residue was dissolved in water (100 mL)
  3. extractionextracted with CH2Cl2 (100 mL×3)
  4. washThe combined organic phases were washed with brine (150 mL)
  5. dry with materialdried over anhydrous Na2SO4
  6. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-ae6ec9c3bee54ec0aec43474a3191766
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09434695B2

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