تفاعل #2446137
ord-6b3cb258f4b14ac09d8fca16680e5f4d
معادلة التفاعل
الكواشف
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المعالجة
- 1درجة الحرارةthe mixture was refluxed for 1 h
- 2workup.ADDITIONwas poured into 500 ml
- 3استخلاصextracted with ethyl acetate (3×150 ml)
- 4غسيلAfter washing with 1N HCl and brine
- 5تجفيفdrying over MgSO4 the solvent
- 6أخرىwas removed under reduced pressure
- 7أخرىthe crude product was obtained as a pale yellow solid
- 8درجة الحرارةOn cooling
- 9استخلاصExtraction with ethyl acetate (3×200 ml)
- 10تجفيفby drying over MgSO4 and removal of the solvent
- 11أخرىgave a yellow solid, which
- 12أخرىwas 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.