2-Chloro-1,1,1,4,4,4-hexafluoro-2-butene → 1,1,1,4,4,4-Hexafluorobutane
反応式
[F:1][C:2]([F:11])([F:10])[C:3](Cl)=[CH:4][C:5]([F:8])([F:7])[F:6].[OH-].[K+]>C(O)C.[Ni]>[F:1][C:2]([F:11])([F:10])[CH2:3][CH2:4][C:5]([F:8])([F:7])[F:6]参加物
5
実験手順
40 g (0.2 mol) of 1,1,1,4,4,4-hexafluoro2-chloro-2-butene were hydrogenated in 300 ml of ethanol in the presence of 12 g of potassium hydroxide and 24 g of Raney nickel in the pressure range of from 20 to 40 bar and at a temperature from 20°to 100° C. The solid components were filtered off, the solvent was extracted with water, and the organic phase was separated and purified by distillation to give 15.5 g (47% of theory) of 1,1,1,4,4,4-hexafluorobutane. The boiling point was 25°to 27° C. at 1013 mbar.
後処理
- filtrationThe solid components were filtered off
- extractionthe solvent was extracted with water
- customthe organic phase was separated
- distillationpurified by distillation
出典と根拠
- ORDレコード
- ord-6292177f9c5e4a16a060a088c3cc2237
- 出典データセット
- uspto-grants-1990_02
- 特許番号
- US04902839
反応ノート
読み込み中…