반응 #46936

ord-d0753003c59d4de69ac40f105885fc62

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타was collected
  2. 2
    workup.DISTILLATIONwere distilled off (1.2 liter)
  3. 3
    기타When most of the volatiles had been removed
  4. 4
    기타to assist in removal of residual toluene
  5. 5
    workup.DISSOLUTIONIn the same flask, the residue was dissolved in 1.2 liter of acetonitrile
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    온도The mixture was heated slowly
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    온도to gentle reflux overnight
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    workup.DISTILLATIONAfter distilling off most of the acetonitrile
  9. 9
    온도cooling
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    workup.ADDITION1.2 liter of water was added
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    온도heated
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    온도to reflux for 30 minutes
  13. 13
    추출Extracted with ether after the mixture
  14. 14
    온도was cooled (200 mL×3)
  15. 15
    건조Combined ether layer was dried over sodium sulfate
  16. 16
    기타The crude product, after removing the solvent
  17. 17
    workup.DISTILLATIONwas purified by vacuum distillation
  18. 18
    기타73-78° C., 6.7 mmHg, Yield: 156 grams (59% for two steps)

실험 절차

Into a 2 liter round bottom flask, equipped with Dean-Stark water separator, cyclohexanone (186 g, 1.90 moles, Aldrich) was dissolved in 1 liter toluene, and then pyrrolidine (292 g, 4.1 moles) was added. The mixture was brought to reflux overnight, during which 55 mL of water was collected. After switching to a distillation head, excess pyrrolindine and toluene were distilled off (1.2 liter). When most of the volatiles had been removed, aspirator vacuum was applied to assist in removal of residual toluene. In the same flask, the residue was dissolved in 1.2 liter of acetonitrile. Allyl bromide (305 g, 2.5 moles) was added dropwise. The mixture was heated slowly to gentle reflux overnight. After distilling off most of the acetonitrile and cooling, 1.2 liter of water was added and heated to reflux for 30 minutes. Extracted with ether after the mixture was cooled (200 mL×3). Combined ether layer was dried over sodium sulfate. The crude product, after removing the solvent, was purified by vacuum distillation: 73-78° C., 6.7 mmHg, Yield: 156 grams (59% for two steps). See also, Stork et al., J. American Chem. Soc., 85:207-222 (1963), and Johnson et al., J. American Chem. Soc., 88:149-159 (1966).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741375B2uspto-grants-2010_06