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HRID 67128作成日:2026年10月25日

Water → 1,1,1-Trifluoro-2-phenyl-5-methyl-hexa-2,4-diene

https://huagongshe.com/reaction/67128

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2,2,2-TrifluoroacetophenoneHCID 9905—
反応物(3-Methylbut-2-enyl)triphenylphosphonium bromideHCID 3083722—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物1,1,1-Trifluoro-2-phenyl-5-methyl-hexa-2,4-dieneHCID 5377803956.6%

反応手順

65 ml of 15% strength solution of n-butyl-lithium in hexane were added dropwise to a suspension of 41.1 g (0.1 mol) of dry 3,3-dimethylallyl-triphenyl-phosphonium bromide in 300 ml of anhydrous tetrahydrofuran at 0° C. under nitrogen, while stirring. The deep red solution thus obtained was stirred at 0° C. for a further 15 minutes and 17.4 g (0.1 mol) of ≃,≃,≃-trifluoroacetophenone were then added dropwise at 0°-10° C. The mixture was subsequently stirred at room temperature until it was decolorized (about 12 hours). 600 ml of water were then added and the reaction mixture was extracted 5 times with 200 ml of petroleum ether each time. The petroleum ether phases were dried over magnesium sulphate and the solvent was then stripped off in a rotary evaporator under a waterpump vacuum. 150 ml of n-hexane were added to the residue and residual triphenyl-phosphine oxide was filtered off. The solvent was subsequently distilled off from the filtrate under normal pressure and the oily residue was then distilled in vacuo. 12.8 g (56.6% of theory) of 1,1,1-trifluoro-2-phenyl-5-methyl-hexa-2,4-diene were obtained as a slightly reddish liquid with a boiling point of 80°-85° C. under 3 mbar.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04344963
出典データセットuspto-grants-1982_08
ORD IDord-b6b0f43275b54e96b3774dc604e5bc7a
出典メモuspto-grants-1982_08