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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67128생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/67128

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2,2,2-TrifluoroacetophenoneHCID 9905—
반응물(3-Methylbut-2-enyl)triphenylphosphonium bromideHCID 3083722—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물1,1,1-Trifluoro-2-phenyl-5-methyl-hexa-2,4-dieneHCID 5377803956.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04344963
출처 데이터셋uspto-grants-1982_08
ORD IDord-b6b0f43275b54e96b3774dc604e5bc7a
출처 메모uspto-grants-1982_08