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HRID 1019426作成日:2026年10月25日

Phosphorus oxychloride → 2,5-Dichloro-1,1,1,6,6,6-hexafluoro-3,4-diazahexa-2,4-diene

https://huagongshe.com/reaction/1019426

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus oxychlorideHCID 24813—
反応物Benzenamine, N,N-diethyl-, hydrochloride (1:1)HCID 79988—
反応物2,2,2-Trifluoro-N'-(trifluoroacetyl)acetohydrazideHCID 229754—
生成物2,5-Dichloro-1,1,1,6,6,6-hexafluoro-3,4-diazahexa-2,4-dieneHCID 7316673053%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08715395B2
出典データセットuspto-grants-2014_05
ORD IDord-c889eed52bd1489b94c9a590baa4b2b3
出典メモuspto-grants-2014_05