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HRID 1031787作成日:2026年10月25日

2-Chloro-1,1,1,4,4,4-hexafluoro-2-butene → 1,1,1,4,4,4-Hexafluorobutane

https://huagongshe.com/reaction/1031787

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-1,1,1,4,4,4-hexafluoro-2-buteneHCID 9815—
反応物Potassium HydroxideHCID 14797—
触媒NickelHCID 935—
溶媒EthanolHCID 702—
生成物1,1,1,4,4,4-HexafluorobutaneHCID 6789047%

反応手順

40 g (0.2 mol) of 1,1,1,4,4,4-hexafluoro-2-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04954666
出典データセットuspto-grants-1990_09
ORD IDord-41dd66b173a54ede8e44abb5b4f74e19
出典メモuspto-grants-1990_09