반응 #72454

ord-ee237da8205243208de063c1c1dd0743

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the mixture was refluxed for 1 h
  2. 2
    workup.ADDITIONwas poured into 500 ml
  3. 3
    추출extracted with ethyl acetate (3×150 ml)
  4. 4
    세척After washing with 1N HCl and brine
  5. 5
    건조drying over MgSO4 the solvent
  6. 6
    기타was removed under reduced pressure
  7. 7
    기타the crude product was obtained as a pale yellow solid
  8. 8
    온도On cooling
  9. 9
    추출Extraction with ethyl acetate (3×200 ml)
  10. 10
    건조by drying over MgSO4 and removal of the solvent
  11. 11
    기타gave a yellow solid, which
  12. 12
    기타was purified by crystallization from acetone/ether

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08541404B2uspto-grants-2013_09