Acetic Acid → 2-(4-bromophenyl)-1H-imidazole

HRID 538977Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 538977
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1.C[O-].[Na+].CO[CH:15](OC)[CH2:16][NH2:17].C(O)(=O)C.Cl>CO>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]2[NH:17][CH:16]=[CH:15][N:7]=2)=[CH:4][CH:3]=1

Komponenten

7

Versuchsvorschrift

To a solution of 4-bromobenzonitrile (80.0 g, 440 mmol) in MeOH (800 mL) was added NaOMe (20.1 mL, 87.9 mmol). The mixture was allowed to stir at ambient temperature for 5.5 hours. 2,2-Dimethoxyethanamine (61.6 mL, 571 mmol) was added followed by acetic acid (50.3 mL, 879 mmol). The reaction mixture was heated to 50° C. for 1 hour and then cooled to ambient temperature. MeOH (200 mL) and HCl (200 mL, 1200 mmol) were added, and the reaction mixture was heated to 65° C. for 18 hours. The reaction mixture was then concentrated, and washed with 1:1 H2O:Et2O (2000 mL). The pH of the aqueous layer was adjusted to pH=9 with 6 N NaOH. The resulting solid was filtered and dried to give 2-(4-bromophenyl)-1H-imidazole (20.0 g, 20%). LCMS (APCI+) m/z 223, 224 [M+H]+.

Aufarbeitung

  1. temperatureThe reaction mixture was heated to 50° C. for 1 hour
  2. temperaturecooled to ambient temperature
  3. temperaturethe reaction mixture was heated to 65° C. for 18 hours
  4. concentrationThe reaction mixture was then concentrated
  5. washwashed with 1:1 H2O
  6. filtrationThe resulting solid was filtered
  7. customdried

Quellen und Nachweise

ORD-Eintrag
ord-c17535fa13d04d88844766be6cfad0ab
Quelldatensatz
uspto-grants-2014_10
Patentnummer
US08865726B2

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