Reaktion #9015

ord-db2fd0075fa6482e8c3b42e6ac372ca6

Reaktionsgleichung

COS(=O)(=O)OC
dimethyl sulfate
Cc1ccc(C#N)c(O)c1
2-Hydroxy-4-methylbenzonitrile
O.[Li+].[OH-]
lithium hydroxide monohydrate
COc1cc(C)ccc1C#N
2-methoxy-4-methylbenzonitrile
Ausbeute 90.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto reflux for 2 hours
  2. 2
    Waschenwashed with saturated aqueous NaHCO3 (3×15 mL)
  3. 3
    Trocknendried (MgSO4)
  4. 4
    Einengenconcentrated
  5. 5
    SonstigePurification of the crude material by column chromatography on silica gel (4:1 hexanes-EtOAc)

Vorschrift

To a solution of 2-Hydroxy-4-methylbenzonitrile (0.46 g, 3.46 mmol) in THF (17 mL) was added lithium hydroxide monohydrate (0.292 g, 6.95 mmol) followed by dimethyl sulfate (0.50 mL, 5.28 mmol). The resultant mixture was heated to reflux for 2 hours then cooled to room temperature. The mixture was diluted with diethyl ether (50 mL), washed with saturated aqueous NaHCO3 (3×15 mL), dried (MgSO4) and concentrated. Purification of the crude material by column chromatography on silica gel (4:1 hexanes-EtOAc) provided 0.456 g (90%) of 2-methoxy-4-methylbenzonitrile as a white solid. 1H NMR (CDCl3) δ 2.41 (s, 3H), 3.91 (s, 3H), 6.77 (s, 1H), 6.81 (d, 1H, J=6Hz), 7.43 (d, 1H, J=6 Hz). ES-MS m/z 148 (M+H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091217B2uspto-grants-2006_08