Ethanol → (3-Bromo-4-methylphenyl)methanamine

HRID 564493Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 564493
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[CH3:11])[C:5]([NH2:7])=O.C(O)C>C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]([CH2:5][NH2:7])[CH:8]=[CH:9][C:10]=1[CH3:11]

Komponenten

4

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

To 3-bromo-4-methylbenzamide (2.14 g, 10 mmol) in THF (10 mL) was added borane dimethyl sulfide complex (2 mL, 20 mmol) at 0° C. The mixture was then heated to 50° C. for 16 h. Additional borane dimethyl sulfide complex (1 mL, 10 mmol) was added and heating continued at 60° C. for an additional 5 days. The reaction was cooled to room temperature and ethanol was cautiously added. When bubbling ceased, 1N HCl was added until pH was ˜2. The mixture was stirred at 50° C. for 4 h. The mixture was partitioned between EtOAc and water. The aqueous was washed 3× with EtOAc. The aqueous was then adjusted to pH 10 with 2N NaOH and extracted 3× with EtOAc. The combined organics phases were dried over anhydrous Na2SO4, filtered, and concentrated to afford the title compound. LC-MS m/z 199.8 (M+H)+, 1.01 min (ret time).

Aufarbeitung

  1. additionAdditional borane dimethyl sulfide complex (1 mL, 10 mmol) was added
  2. temperatureheating
  3. temperatureThe reaction was cooled to room temperature
  4. customWhen bubbling
  5. addition1N HCl was added until pH was ˜2
  6. customThe mixture was partitioned between EtOAc and water
  7. washThe aqueous was washed 3× with EtOAc
  8. extractionextracted 3× with EtOAc
  9. dry with materialThe combined organics phases were dried over anhydrous Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-40efc2375ef84fd7a4af6d0aecf3d6d0
Quelldatensatz
uspto-grants-2011_11
Patentnummer
US08067408B2

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