반응 #94255

ord-fa605c18c67c4c4f80dcb5deb8ca8779

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타round-bottomed flask was equipped with a mechanical stirrer
  2. 2
    온도reflux condenser
  3. 3
    workup.ADDITIONsurmounted by calcium chloride drying tube, addition funnel
  4. 4
    기타was placed in a water bath at 221
  5. 5
    기타2 ° C
  6. 6
    기타did not rise over 23° C
  7. 7
    기타Reaction
  8. 8
    workup.WAITthe reaction was completed after another 3 days
  9. 9
    기타was withdrawn from the reaction mixture
  10. 10
    workup.WAITto stand for 15 minutes
  11. 11
    여과The quinoline hydrochloride was filtered off
  12. 12
    세척washed with 25 ml pentane which
  13. 13
    workup.ADDITIONwas added to the pentane solution
  14. 14
    세척This solution was then successively washed with 25 ml
  15. 15
    건조portions of water, and finally dried over sodium sulfate
  16. 16
    기타After removal
  17. 17
    건조of drying agent and pentane
  18. 18
    기타was obtained

실험 절차

A four-necked 500 ml. round-bottomed flask was equipped with a mechanical stirrer, reflux condenser surmounted by calcium chloride drying tube, addition funnel and thermometer. A solution of 19 g. (0.1 mole) 1,3-dimethyl-3-(t-butylperoxy)butyl alcohol and 13.3 g (slightly over 0.1 mole) quinoline in 250 ml. pentane was placed in the flask which was placed in a water bath at 221/2 ° C. Then 12.3 g (0.1 mole) isopropyl chloroformate was added dropwise over 5 minutes; the temperature did not rise over 23° C. Reaction was not complete after 3 days. Another 3 g. of quinoline was added, and the reaction was completed after another 3 days as indicated by the fact that no further precipitate of quinoline hydrochloride formed when an aliquot of clean pentane solution was withdrawn from the reaction mixture and allowed to stand for 15 minutes. The quinoline hydrochloride was filtered off and washed with 25 ml pentane which was added to the pentane solution. This solution was then successively washed with 25 ml. of 7% hydrochloric acid, two 50 ml. portions of water, and finally dried over sodium sulfate. After removal of drying agent and pentane, a yield of 23.8 g. (86.4%) of material found to be 1,3-dimethyl-3-(t-butylperoxy)butyl isopropyl carbonate by infrared analysis, was obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04129700uspto-grants-1978_12