Réaction #1605777

ord-f5c24dac11c6453ca71999cdc77cb7c5

Équation de réaction

Cc1ccc(C(N)=O)c(O)c1
2-hydroxy-4-methyl-benzamide
O=C([O-])[O-].[K+].[K+]
K2CO3
COS(=O)(=O)OC
Me2SO4
COc1cc(C)ccc1C(N)=O
2-methoxy-4-methyl-benzamide

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas heated
  2. 2
    workup.ADDITIONwas added at that temperature
  3. 3
    TempératureThe resulting mixture was refluxed overnight
  4. 4
    FiltrationThe reaction mixture was then filtered
  5. 5
    Concentrationthe filtrate was concentrated
  6. 6
    workup.DISSOLUTIONThe resulting residue was dissolved in 1000 mL of methanol/ammonia (1:1)
  7. 7
    AutreAfter removal of the solvent
  8. 8
    Autrethe residue was recrystallized from EtOAc/PE

Mode opératoire

A mixture of 2-hydroxy-4-methyl-benzamide (15.1 g, 0.1 mol) and K2CO3 (41.7 g, 0.3 mol) in 1000 mL of acetone was heated to reflux for 1 hour before Me2SO4 was added at that temperature. The resulting mixture was refluxed overnight. The reaction mixture was then filtered and the filtrate was concentrated. The resulting residue was dissolved in 1000 mL of methanol/ammonia (1:1) and stirred at room temperature for 3 hours. After removal of the solvent, the residue was recrystallized from EtOAc/PE to afford 102 g of 2-methoxy-4-methyl-benzamide (yield 61%). 1H NMR (400 MHz, DMSO-d6): δ 7.72 (d, J=7.6 Hz, 1H), 7.57 (br s, 1H), 7.46 (br s, 1H), 6.92 (s, 1 H), 6.81 (d, J=7.6 Hz, 1 H), 3.85 (s, 3H), 2.31 (s, 3H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09072313B2uspto-grants-2015_07