반응 #586105

ord-4d9a9293694846f2b7df498efe5dd4fb

반응 방정식

CC1=C(O[Si](C)(C)C)CCC1=O
2-methyl-3-(trimethylsilyloxy)cyclopent-2-enone
N
ammonia
[Li][CH2]CCC
n-butyllithium
Cl
hydrochloric acid
Brc1cccc2cccnc12
8-bromoquinoline
CC1=C(c2cccc3cccnc23)CCC1=O
2-methyl-3-(8-quinolyl)cyclopent-2-enone
수율 74.9%

반응 조건

온도
-80°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThe mixture was stirred for a further 15 minutes
  2. 2
    workup.STIRRINGwhile stirring
  3. 3
    온도to warm to room temperature
  4. 4
    workup.STIRRINGwhile stirring
  5. 5
    workup.STIRRINGwas stirred for a further one hour
  6. 6
    기타the mixture obtained in this way
  7. 7
    온도was refluxed for 3 hours
  8. 8
    온도to cool to room temperature
  9. 9
    workup.STIRRINGwhile stirring
  10. 10
    기타The aqueous phase was then separated off from the organic phase
  11. 11
    추출the aqueous phase was extracted twice with diethyl ether
  12. 12
    건조dried over magnesium sulfate
  13. 13
    여과filtered
  14. 14
    workup.DISTILLATIONthe solvent was distilled off
  15. 15
    기타The residue obtained in this way
  16. 16
    workup.DISTILLATIONwas distilled at 119-139° C.

실험 절차

A mixture of 38.7 g (186 mmol) of 8-bromoquinoline in 250 ml of tetrahydrofuran was cooled to −80° C. and 74.4 ml of n-butyllithium (2.5 M in hexane, 186 mmol) were subsequently added while stirring. The mixture was stirred for a further 15 minutes and, while stirring, 49.9 g (186 mmol) of 2-methyl-3-(trimethylsilyloxy)cyclopent-2-enone were added. The mixture was allowed to warm to room temperature while stirring and was stirred for a further one hour. The reaction mixture was then hydrolyzed by means of a mixture of 40 g of ice and 30 ml of concentrated hydrochloric acid and the mixture obtained in this way was refluxed for 3 hours. The mixture was allowed to cool to room temperature while stirring and ammonia solution was added until the pH was 12. The aqueous phase was then separated off from the organic phase and the aqueous phase was extracted twice with diethyl ether. The organic phases were combined, dried over magnesium sulfate, filtered and the solvent was distilled off. The residue obtained in this way was distilled at 119-139° C. and 2×10−2 mbar to give 31.1 g (139.3 mmol, 74.9%) of 2-methyl-3-(8-quinolyl)cyclopent-2-enone.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07767613B2uspto-grants-2010_08