تفاعل #2446138
ord-b6327e1630f1406893d76bd22aa6c37e
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المتفاعلات
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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
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 1,2,3,4-tetrahydroquinoline (26.6 g, 0.20 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 minutes. 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 1,2,6,7-tetrahydro-5H-pyrido[3,2,1-ij]quinolin-3-one (15.6 g, 83.3 mmol, 88%) as a yellow solid.