Reaktion #1669462

ord-26a7987071d54cbb872ce65ae9f9d654

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto reflux for 1 hour
  2. 2
    Waschenwashed with saturated aqueous NaHCO3 (4×10 mL)
  3. 3
    Trocknendried (MgSO4)
  4. 4
    Einengenconcentrated
  5. 5
    SonstigePurification of the crude material by column chromatography on silica gel (9:1 hexanes-EtOAc)

Vorschrift

To a solution of ethyl 6-methylsalicylate (1.27 g, 6.97 mmol) in THF (35 mL) was added lithium hydroxide monohydrate (0.594 g, 14.2 mmol) followed by dimethyl sulfate (1.00 mL, 10.6 mmol). The resultant mixture was heated to reflux for 1 hour then cooled to room temperature. The mixture was diluted with diethyl ether (70 mL), washed with saturated aqueous NaHCO3 (4×10 mL), dried (MgSO4) and concentrated. Purification of the crude material by column chromatography on silica gel (9:1 hexanes-EtOAc) provided 1.23 g (91%) of ethyl 2-methoxy-6-methylbenzoate as a white solid. 1H NMR (CDCl3) δ1.38 (t, 3H, J=7.2 Hz), 2.30 (s, 3H), 3.82 (s, 3H), 4.40 (q, 2H, J=7.2 Hz), 6.76 (d, 1H, J=8.4 Hz), 6.79 (d, 1H, J=7.8 Hz), 7.23 (dd, 1H, J=7.8, 8.4 Hz).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06734191B2uspto-grants-2004_05