Reaktion #72454

Reaktionsgleichung

AlCl3

NaCl

aluminum chloride

hydrochloric acid

3-chloropropanoyl chloride

indoline

HCl

→

1,2,5,6-tetrahydro-pyrrolo[3,2,1-ij]quinolin-4-one

Ausbeute 69.3%

Lösungsmittel

water

acetone

acetone

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturthe mixture was refluxed for 1 h
2. 2
   workup.ADDITIONwas poured into 500 ml
3. 3
   Extraktionextracted with ethyl acetate (3×150 ml)
4. 4
   WaschenAfter washing with 1N HCl and brine
5. 5
   Trocknendrying over MgSO4 the solvent
6. 6
   Sonstigewas removed under reduced pressure
7. 7
   Sonstigethe crude product was obtained as a pale yellow solid
8. 8
   TemperaturOn cooling
9. 9
   ExtraktionExtraction with ethyl acetate (3×200 ml)
10. 10
    Trocknenby drying over MgSO4 and removal of the solvent
11. 11
    Sonstigegave a yellow solid, which
12. 12
    Sonstigewas purified by crystallization from acetone/ether

Vorschrift

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.

Quelle