Reaktion #82396

ord-c15444310c7749b6894e111ab9d0b890

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheated at 100° C. for 0.25 h
  2. 2
    workup.ADDITIONwas added to the reaction mixture
  3. 3
    SonstigeThe precipitate which formed
  4. 4
    Filtrationwas filtered
  5. 5
    Waschenwashed with 3×75 mL of water
  6. 6
    workup.DISSOLUTIONdissolved in 300 mL of methylene chloride
  7. 7
    TrocknenThe methylene chloride solution was dried over anhydrous magnesium sulfate
  8. 8
    Filtrationfiltered
  9. 9
    Einengenconcentrated

Vorschrift

4-(2',3'-Dimethoxyphenyl)-3-phenylbutyric acid (37 g, 123 mmol), from Step 5, was added dropwise to 200 g of polyphosphoric acid heated to 100° C. The resultant mixture was stirred and heated at 100° C. for 0.25 h. A mixture of 100 g of ice and 200 mL of water was added to the reaction mixture. The precipitate which formed was filtered, washed with 3×75 mL of water and dissolved in 300 mL of methylene chloride. The methylene chloride solution was dried over anhydrous magnesium sulfate, filtered and concentrated to give 28 g (81% yield) of 5,6-dimethoxy-3-phenyl-1,2,3,4-tetrahydronaphthalen-1-one, m.p; 127°-128° C.; 1H NMR (CDCl3) δ: 2.75-3.0 (m, 3H), 3.3-3.5 (m, 2H), 3.8 (s, 3H), 3.95 (s, 3H), 693 (d, 1H), 7.25-7.4 (m, 5H), 7.9 (d, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05621133uspto-grants-1997_04