Hydrochloric Acid → 2-Methoxy-4-methylbenzenemethanamine

HRID 1686124Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1686124
[CH3:1][O:2][C:3]1[CH:11]=[C:10]([CH3:12])[CH:9]=[CH:8][C:4]=1[C:5]([NH2:7])=O.B.O1CCCC1.Cl.O>C1COCC1>[CH3:1][O:2][C:3]1[CH:11]=[C:10]([CH3:12])[CH:9]=[CH:8][C:4]=1[CH2:5][NH2:7]

Komponenten

6

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a solution of 2-methoxy-4-methylbenzamide (14.55 g, 88.08 mmol) in dry THF (50 mL) was added dropwise Borane-tetrahydrofuran complex (1.0 M in THF, 220 mL, 2.5 eq) at 0° C. under N2 atmosphere. The reaction mixture was then heated to 60° C. overnight. The reaction was cooled to room temperature, aq. HCl (6 N, 37 mL) was added carefully and the reaction mixture was then heated at 70° C. for 2 hrs. After cooling, water was added and the resulting solution was washed with ether. The aqueous layer was basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3 then extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated to give 8.5 g of (2-methoxy-4-methylphenyl)methanamine. (64% yield)

Aufarbeitung

  1. temperatureThe reaction was cooled to room temperature
  2. temperaturethe reaction mixture was then heated at 70° C. for 2 hrs
  3. temperatureAfter cooling
  4. washthe resulting solution was washed with ether
  5. customwas basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3
  6. extractionthen extracted with ethyl acetate
  7. washThe organic layer was washed with brine
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-34eb81c691bd47b19c943fd3c8e8e348
Quelldatensatz
uspto-grants-2012_04
Patentnummer
US08148536B2

Notizen zur Reaktion

Wird geladen…