تفاعل #5690

ord-9e54ac87e6cd4333953c4b9787bd6f06

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةheated
  2. 2
    درجة الحرارةunder reflux for 43 hours
  3. 3
    استخلاصextracted with 150 mL of ether
  4. 4
    غسيلThe extract was washed with H2O (2×50 mL) and 50 mL of brine
  5. 5
    تجفيفdried over MgSO4
  6. 6
    أخرىThe oil was chromatographed on the solvent
  7. 7
    workup.WAITleft 35.7 g of brown oil
  8. 8
    أخرىThe oil was chromatographed on a 1100 g column of silica gel
  9. 9
    غسيلThe column was eluted with 25% CH2Cl2 -Skellysolve B and 200 mL fractions
  10. 10
    أخرىwere collected

الإجراء التجريبي

A mixture of 17.57 g (0.15 mole) of indole, 23.55 g (0.15 mole) of bromobenzene, 21 g of anhydrous potassium carbonate, 0.75 g of CuO, and 30 mL of DMF was stirred and heated under reflux for 43 hours. The cooled mixture was diluted with 200 mL of H2O and extracted with 150 mL of ether. The extract was washed with H2O (2×50 mL) and 50 mL of brine and dried over MgSO4. The oil was chromatographed on the solvent left 35.7 g of brown oil. The oil was chromatographed on a 1100 g column of silica gel. The column was eluted with 25% CH2Cl2 -Skellysolve B and 200 mL fractions were collected. The fractions were assayed by silica gel tlc (1×4") (25% CH2Cl2 -Skellysolve B). Fractions 15-22 were combined giving 5.86 g (20%) of 1-phenylindole as a yellow oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05245046uspto-grants-1993_09