تفاعل #6292

ord-7ba62443ec7649e18842d3f4e41dec27

معادلة التفاعل

O=C(c1ccccc1)C(F)(F)F
trifluoroacetophenone
O=S(=O)(O)C(F)(F)F
trifluoromethane sulfonic acid
COc1ccccc1
anisole
Br
hydrobromic acid
Oc1ccc(C(c2ccccc2)(c2ccc(O)cc2)C(F)(F)F)cc1
1,1-bis(4-hydroxyphenyl)-1-phenyl-2,2,2-trifluoroethane

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe mixture is then transferred to a separatory funnel
  2. 2
    غسيلthe organic material is washed with water (3×11), saturated bicarbonate (3×500 ml) and water (2×500 ml)
  3. 3
    أخرىThe organic phase is dried
  4. 4
    أخرىthe volatiles removed in vacuo
  5. 5
    أخرىThe resulting material is crystallized from aqueous methanol
  6. 6
    درجة الحرارةThe mixture is cooled
  7. 7
    workup.ADDITIONpoured
  8. 8
    أخرىover crushed ice
  9. 9
    أخرىthe solid collected
  10. 10
    أخرىThe crude material is recrystallized from ethanol and petroleum ether

الإجراء التجريبي

A mixture of 100 grams (0.57 mol) of trifluoroacetophenone, 100 grams (0.7 mol) trifluoromethane sulfonic acid, and 100 grams (10.9 mol) anisole is stirred at room temperature for 24 hours. The mixture is then transferred to a separatory funnel and the organic material is washed with water (3×11), saturated bicarbonate (3×500 ml) and water (2×500 ml). The organic phase is dried and the volatiles removed in vacuo. The resulting material is crystallized from aqueous methanol. 37.2 grams (0.1 mol) of this product is refluxed with glacial acetic acid saturated with anhydrous hydrobromic acid. The mixture is cooled and poured over crushed ice and the solid collected. The crude material is recrystallized from ethanol and petroleum ether to give 1,1-bis(4-hydroxyphenyl)-1-phenyl-2,2,2-trifluoroethane.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05247050uspto-grants-1993_09