تفاعل #6615

ord-4f4f202b0c7649758da42a8dec41db76

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe cooling bath is removed
  2. 2
    أخرىThe benzene is removed under reduced pressure
  3. 3
    أخرىprovides a residue which
  4. 4
    غسيلwashed with saturated ammonium chloride
  5. 5
    تركيزThe ether layer is concentrated under reduced pressure

الإجراء التجريبي

To a cooled solution (0° C.) of the epoxide from Example 1, Step A above (32.7 g, 125 mmol) in benzene (200 ml) is added dropwise 7.6 ml BF3 ·OEt2 (62 mmol). The cooling bath is removed and the reaction mixture warmed to room temperature and stirred for 2 hours. The benzene is removed under reduced pressure and provides a residue which is dissolved in ether (300 ml) and washed with saturated ammonium chloride. The ether layer is concentrated under reduced pressure to provide 26 g (80%) of 2-(4-fluoro-3-methylphenyl)-4,4,6,6-tetramethylcyclohexanone. The ketone is recrystallized from pentane to give a white solid; m.p. 63°-64° C.: 1H NMR δ=1.05 (s,3), 1.1 (s,3), 1.3 (s,3), 1.32 (s,3), 1.75 (s,2), 2.0 (q,2), 2.3 (s,3), 3.95 (dd,1), 6.95 (m,3).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05248830uspto-grants-1993_09