تفاعل #2446137

ord-6b3cb258f4b14ac09d8fca16680e5f4d

معادلة التفاعل

[Al+3].[Cl-].[Cl-].[Cl-]
AlCl3
[Cl-].[Na+]
NaCl
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
Cl
hydrochloric acid
O=C(Cl)CCCl
3-chloropropanoyl chloride
c1ccc2c(c1)CCN2
indoline
Cl
HCl
O=C1CCc2cccc3c2N1CC3
1,2,5,6-tetrahydro-pyrrolo[3,2,1-ij]quinolin-4-one
المردود 69.3%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was refluxed for 1 h
  2. 2
    workup.ADDITIONwas poured into 500 ml
  3. 3
    استخلاصextracted with ethyl acetate (3×150 ml)
  4. 4
    غسيلAfter washing with 1N HCl and brine
  5. 5
    تجفيفdrying over MgSO4 the solvent
  6. 6
    أخرىwas removed under reduced pressure
  7. 7
    أخرىthe crude product was obtained as a pale yellow solid
  8. 8
    درجة الحرارةOn cooling
  9. 9
    استخلاصExtraction with ethyl acetate (3×200 ml)
  10. 10
    تجفيفby drying over MgSO4 and removal of the solvent
  11. 11
    أخرىgave a yellow solid, which
  12. 12
    أخرىwas purified by crystallization from acetone/ether

الإجراء التجريبي

A solution of 3-chloropropanoyl chloride (9.1 ml, 95.0 mmol) in 20 ml dry acetone was added dropwise to a solution of indoline (20.5 g, 0.21 mol) in 80 ml dry acetone and the mixture was refluxed for 1 h. After cooling to ambient temperature the solution was poured into 500 ml stirred 2N HCl and extracted with ethyl acetate (3×150 ml). After washing with 1N HCl and brine and drying over MgSO4 the solvent was removed under reduced pressure and the crude product was obtained as a pale yellow solid. This was added portionwise to a molten mixture of AlCl3 (60.0 g, 0.45 mol) and NaCl (17.5 g, 300 mmol) at 150° C. and stirred for additional 30 min. On cooling, excess aluminum chloride was decomposed by the addition of a chilled mixture of 20 ml concentrated hydrochloric acid and 500 ml water. Extraction with ethyl acetate (3×200 ml), followed by drying over MgSO4 and removal of the solvent gave a yellow solid, which was purified by crystallization from acetone/ether yielding 1,2,5,6-tetrahydro-pyrrolo[3,2,1-ij]quinolin-4-one (11.8 g, 65.8 mmol, 69%) as colorless needles.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08685960B2uspto-grants-2014_04