Vinylidene fluoride → 2-Trifluoromethyl-1,1,1,2,4,4-hexafluorobutane
反応式
[F:1][C:2]([F:13])([F:12])[CH:3]([CH2:8][CH:9]([F:11])[F:10])[C:4]([F:7])([F:6])[F:5].[F:14]C(F)=C>>[F:1][C:2]([F:12])([F:13])[C:3]([F:14])([CH2:8][CH:9]([F:10])[F:11])[C:4]([F:6])([F:5])[F:7]参加物
3
実験手順
As another example, 2-trifluoromethyl-1,1,1,4,4-pentafluorobutane may be prepared by reacting commercially available 1,1-difluoroethylene according to the procedure of George L. Fleming et al., supra, to form a product which may then be hydrogenated to form 2-trifluoromethyl-1,1,1,2,4,4-hexafluorobutane which may then be dehydrohalogenated and then hydrogenated to form 2-trifluoromethyl-1,1,1,4,4-pentafluorobutane.
後処理
- customFleming et al., supra, to form a product which
出典と根拠
- ORDレコード
- ord-00d582b5a898438da9c68dcac2bacc2c
- 出典データセット
- uspto-grants-1992_07
- 特許番号
- US05130345
反応ノート
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