تفاعل #1106608

ord-c889eed52bd1489b94c9a590baa4b2b3

معادلة التفاعل

CCN(CC)c1ccccc1.Cl
N,N-diethylaniline hydrochloride
O=C(NNC(=O)C(F)(F)F)C(F)(F)F
1,2-bis(trifluoroacetyl)hydrazine
O=P(Cl)(Cl)Cl
phosphoryl chloride
FC(F)(F)C(Cl)=NN=C(Cl)C(F)(F)F
2,5-dichloro-1,1,1,6,6,6-hexafluoro-3,4-diazahexa-2,4-diene
المردود 53.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىfitted with a condenser
  2. 2
    أخرىleading to a cold trap
  3. 3
    أخرى(−78° C.)
  4. 4
    درجة الحرارةThe mixture was heated
  5. 5
    درجة الحرارةunder reflux for 5 h
  6. 6
    درجة الحرارةto cool
  7. 7
    workup.WAITstored overnight
  8. 8
    أخرىcondensed in the cold trap
  9. 9
    أخرىthe two layers which had formed
  10. 10
    أخرىwere separated
  11. 11
    workup.ADDITIONThe layer was added to ice water (85 mL)
  12. 12
    workup.STIRRINGthe mixture vigorously stirred for 1 h in a flask
  13. 13
    أخرىfitted with a condenser
  14. 14
    أخرىSeparation of the lower organic layer
  15. 15
    أخرىgave the main batch of the crude product (6.4 g)
  16. 16
    أخرىthe organic layer subjected to preliminary purification by trap-to-trap
  17. 17
    workup.DISTILLATIONdistillation in vacuum
  18. 18
    أخرىto afford a second batch of crude product (1.6 g)
  19. 19
    workup.DISTILLATIONDistillation of the combined product through a vacuum-jacketed Vigreux column

الإجراء التجريبي

A mixture of N,N-diethylaniline hydrochloride (18.5 g, 0.1 mol), 1,2-bis(trifluoroacetyl)hydrazine (10.3 g, 0.46 mol) and phosphoryl chloride (160 mL) was stirred for 30 minutes under nitrogen in a flask fitted with a condenser leading to a cold trap (−78° C.). The mixture was heated under reflux for 5 h and then allowed to cool and stored overnight. The flask contents and the small amount of material which had condensed in the cold trap were combined and the two layers which had formed were separated. The layer was added to ice water (85 mL) and the mixture vigorously stirred for 1 h in a flask fitted with a condenser. Separation of the lower organic layer gave the main batch of the crude product (6.4 g). The original dark upper layer was treated similarly with ice water (75 mL) and the organic layer subjected to preliminary purification by trap-to-trap distillation in vacuum to afford a second batch of crude product (1.6 g). Distillation of the combined product through a vacuum-jacketed Vigreux column gave 2,5-dichloro-1,1,1,6,6,6-hexafluoro-3,4-diazahexa-2,4-diene (6.3 g, 53%) as an oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08715395B2uspto-grants-2014_05