تفاعل #50549

ord-279e2ce874524bb798c8e2a40a5e5657

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe solution was heated
  2. 2
    درجة الحرارةat reflux for 18 h
  3. 3
    أخرىevaporated
  4. 4
    استخلاصextracted with ethyl acetate (3×20 mL)
  5. 5
    غسيلwashed with brine
  6. 6
    أخرىdried
  7. 7
    أخرىevaporated
  8. 8
    أخرىThe solid was recrystallized from hexane

الإجراء التجريبي

Nitrogen gas was bubbled through a mixture of the product of part e (0.611 g, 27 mmol) and phenylboric acid (0.36 g, 29 mmol) in 5:2 toluene/ethanol(30 mL) for 4 hours. Sodium carbonate (0.57 g, 5.38 mmol) was added followed by tetrabutylammonium bromide (0.049 g, 0.13 mmol) and tetrakis(triphenylphosphine)palladium (0.012 g, 0.04 mmol). The solution was heated at reflux for 18 h, cooled to room temperature, and evaporated. The residue was taken up in water (50 mL) and extracted with ethyl acetate (3×20 mL). The organics were combined, washed with brine, dried and evaporated. The solid was recrystallized from hexane to provide 0.429 g (70%) of 7-phenylisochroman-4-one as a gold-colored solid, mp 127°-128° C.: 1H NMR (CDCl3) δ8.12 (d, 1H), 7.60-7.66 (m, 3H), 7.39-7.51 (m, 4H), 4.96 (s, 2 H), 4.41 (s, 2H); IR (KBr) 1688 cm-1 ; Mass spectrum m/z=225 (M+H); Anal. calcd. for C15H12O2 : C 80.34, H 5.39; Found: C 80.03, H 5.45.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05428040uspto-grants-1995_06