반응 #549752

ord-45178722cb6b401a9f3c6a4bb09a6d0c

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Into a 100 ml reaction flask
  2. 2
    기타equipped with spin bar
  3. 3
    온도reflux condenser
  4. 4
    온도heating mantle
  5. 5
    workup.ADDITIONSlowly added to the reaction mass over a period of 30 minutes
  6. 6
    온도The reaction mass is then heated
  7. 7
    온도to reflux
  8. 8
    온도refluxed for a period of 9 hours
  9. 9
    기타is removed from the reaction mass
  10. 10
    온도At the end of the 9 hour refluxing period
  11. 11
    온도the reaction mass is then cooled
  12. 12
    기타transferred to a separatory funnel
  13. 13
    세척washed with one 50 ml portion of saturated sodium chloride solution
  14. 14
    건조dried over anhydrous sodium sulfate
  15. 15
    여과filtered
  16. 16
    workup.DISTILLATIONdistilled on a Microvigreux column
  17. 17
    기타yielding the following fractions

실험 절차

Into a 100 ml reaction flask equipped with spin bar, reflux condenser, heating mantle and hot plate with magnetic stirring apparatus is placed 0.2 grams para-toluenesulfonic acid, 5 ml cyclohexane and 4.5 grams of 1,3-butanediol. Slowly added to the reaction mass over a period of 30 minutes is 3-methylthiopropionaldehyde (5.2 grams; 0.05 moles). The reaction mass is then heated to reflux and refluxed for a period of 9 hours. During the refluxing process, water of reaction is removed from the reaction mass. At the end of the 9 hour refluxing period, the reaction mass is then cooled and transferred to a separatory funnel and washed with one 50 ml portion of saturated sodium chloride solution and then dried over anhydrous sodium sulfate, filtered and distilled on a Microvigreux column yielding the following fractions:

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04515966uspto-grants-1985_05