반응 #1884946
ord-efb21ab822bc47e1b70096119275eb88
반응 방정식
시약
반응 조건
후처리
- 1기타fitted with a condenser
- 2기타leading to a cold trap
- 3기타(−78° C.)
- 4온도The mixture was heated
- 5온도under reflux for 5 h
- 6온도to cool
- 7workup.WAITstored overnight
- 8기타condensed in the cold trap
- 9기타the two layers which had formed
- 10기타were separated
- 11workup.ADDITIONThe layer was added to ice water (85 mL)
- 12workup.STIRRINGthe mixture vigorously stirred for 1 h in a flask
- 13기타fitted with a condenser
- 14기타Separation of the lower organic layer
- 15기타gave the main batch of the crude product (6.4 g)
- 16기타the organic layer subjected to preliminary purification by trap-to-trap
- 17workup.DISTILLATIONdistillation in vacuum
- 18기타to afford a second batch of crude product (1.6 g)
- 19workup.DISTILLATIONDistillation of the combined product through a vacuum-jacketed Vigreux column
실험 절차
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.