تفاعل #5691

ord-3ef121dbf1f0400b85825dd9302cc9ce

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةheated at 55°-60° for 24 hours
  2. 2
    أخرىThe layers were separated
  3. 3
    استخلاصThe aqueous layer was extracted with 100 mL of toluene
  4. 4
    غسيلThe combined toluene phases were washed with 2N HCl (2×50 mL), H2O (2×50 mL), and 50 mL of brine
  5. 5
    تجفيفdried over MgSO4
  6. 6
    أخرىEvaporation of the solvent
  7. 7
    workup.WAITleft 32.3 g of dark brown oil
  8. 8
    أخرىThe oil was chromatographed on a 1100 g column of silica gel
  9. 9
    أخرىwere collected

الإجراء التجريبي

A mixture of 19.33 g (0.1 mole) of 2-phenylindole, 13.92 g (0.11 mole) of benzyl chloride, 33 g (0.5 mole) of 85% KOH, 14 mL of H2O, 2.5 g (2.5 mmoles) of PEG-1000, and 100 mL of toluene was stirred and heated at 55°-60° for 24 hours. After cooling to room temperature, 100 mL of H2O was added. The layers were separated. The aqueous layer was extracted with 100 mL of toluene. The combined toluene phases were washed with 2N HCl (2×50 mL), H2O (2×50 mL), and 50 mL of brine and dried over MgSO4. Evaporation of the solvent left 32.3 g of dark brown oil. The oil was chromatographed on a 1100 g column of silica gel. The column was elut4d 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 18-20 were combined giving 3.74 g (13%) of 1-benzyl-2-phenylindole as a solid.

المصدر

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