Réaction #63514

ord-beb59b12eed641519081d3a076ad5d99

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    LavageThe organic layer was washed with dilute HCl (2×300 ml)
  2. 2
    Extractionextracted with CHCl3 (2×500 ml)
  3. 3
    ConcentrationThe dried chloroform layer (MgSO4) was concentrated to an oil
  4. 4
    workup.DISSOLUTIONThe oil was dissolved in ether

Mode opératoire

To a stirred solution of N-acetyl-3-methoxyphenethylamine (96.0 g, 0.497 m) in toluene (600 ml) at 15°-20° C. phosphorus oxychloride (190.5 g, 1.24 m) was added dropwise over 2 hours. The reaction was stirred overnight at room temperature, then poured into 1 liter of ice water. The organic layer was washed with dilute HCl (2×300 ml), and the aqueous layers were combined, basified, and extracted with CHCl3 (2×500 ml). The dried chloroform layer (MgSO4) was concentrated to an oil. The oil was dissolved in ether and acidified with HCl gas to yield 55.9 g of the product, 3,4-dihydro-6-methoxy-1-methylisoquinoline, m.p. 206°-207°.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04766131uspto-grants-1988_08