Réaction #1106608

Équation de réaction

N,N-diethylaniline hydrochloride

1,2-bis(trifluoroacetyl)hydrazine

phosphoryl chloride

→

2,5-dichloro-1,1,1,6,6,6-hexafluoro-3,4-diazahexa-2,4-diene

Rendement 53.0%

Conditions de réaction

Traitement

1. 1
   Autrefitted with a condenser
2. 2
   Autreleading to a cold trap
3. 3
   Autre(−78° C.)
4. 4
   TempératureThe mixture was heated
5. 5
   Températureunder reflux for 5 h
6. 6
   Températureto cool
7. 7
   workup.WAITstored overnight
8. 8
   Autrecondensed in the cold trap
9. 9
   Autrethe two layers which had formed
10. 10
    Autrewere 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
    Autrefitted with a condenser
14. 14
    AutreSeparation of the lower organic layer
15. 15
    Autregave the main batch of the crude product (6.4 g)
16. 16
    Autrethe organic layer subjected to preliminary purification by trap-to-trap
17. 17
    workup.DISTILLATIONdistillation in vacuum
18. 18
    Autreto afford a second batch of crude product (1.6 g)
19. 19
    workup.DISTILLATIONDistillation of the combined product through a vacuum-jacketed Vigreux column

Mode opératoire

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.

Source