تفاعل #5688

ord-6e955e2991c44b43badb9a9ccdf6b729

معادلة التفاعل

N
ammonia
ClCc1ccccc1
benzyl chloride
[NH2-].[Na+]
sodium amide
[Na]
sodium
N
NH3
c1ccc2[nH]ccc2c1
indole
c1ccc(Cn2ccc3ccccc32)cc1
1-Benzylindole

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىto evaporate overnight
  2. 2
    غسيلThe sides of the flask were washed down with MeOH
  3. 3
    workup.ADDITION500 mL of H2O was added
  4. 4
    استخلاصThe mixture was extracted with ether (2×500 mL)
  5. 5
    غسيلThe combined ether extracts were washed with 250 mL of H2O
  6. 6
    تجفيفdried over MgSO4
  7. 7
    أخرىThe solvent was evaporated
  8. 8
    workup.DISTILLATIONThe residue was distilled at 2 mm
  9. 9
    workup.WAITupon standing several hours
  10. 10
    أخرىFraction III was crystallized from aqueous MeOH giving 9.9 g of colorless needles, m.p. 42.5°-43.5°
  11. 11
    أخرىFraction V was crystallized from aqueous MeOH giving 11.6 g of colorless needles, m.p. 43°-45.5°

الإجراء التجريبي

To a stirred mixture of sodium amide (prepared from 19.6 g, 0.85 mole of sodium and a few mg of Fe(NO3)3 -9H2O) and 800 mL of liquid NH3 (a dry ice condenser was used) was added a solution of 100 g (0.85 mole) of indole in 250 mL of dry ether during 15 minutes. The mixture was stirred for 30 minutes and then a solution of 107.8 g (0.85 mole) of benzyl chloride in 100 mL of dry ether was added during 30 minutes. The ammonia was allowed to evaporate overnight. The sides of the flask were washed down with MeOH and then 500 mL of H2O was added. The mixture was extracted with ether (2×500 mL). The combined ether extracts were washed with 250 mL of H2O and dried over MgSO4. The solvent was evaporated. The residue was distilled at 2 mm: fr 1, b.p. 172°- 183°, fr II, b.p. 183°-186°, 5 g; fr III, b.p. 186°-187°, 10.9 g; fr IV, b.p. 187°-191°, 121.8 g; fr V, b.p. 191°-197°, 13.9 g. Fractions III-V solidified upon standing several hours. Fraction IV had m.p. 42°-43°. Fraction III was crystallized from aqueous MeOH giving 9.9 g of colorless needles, m.p. 42.5°-43.5°. Fraction V was crystallized from aqueous MeOH giving 11.6 g of colorless needles, m.p. 43°-45.5°. The total yield was 143.3 g (81.5%).

المصدر

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