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HRID 1634374作成日:2026年10月27日

Carbon Dioxide → 1-Chloro-4-[2,3,3-trifluoro-1-(2-methoxyethyl)-2-propenyl]benzene

https://huagongshe.com/reaction/1634374

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物1-Bromo-1,2,2-trifluoroetheneHCID 11730—
反応物3-(4-Chlorophenyl)-3-bromopropyl methyl etherHCID 12056646—
触媒ZincHCID 23994—
触媒(+)-LimoneneHCID 440917—
溶媒DimethylformamideHCID 6228—
生成物1-Chloro-4-[2,3,3-trifluoro-1-(2-methoxyethyl)-2-propenyl]benzeneHCID 1205664713.1%

反応条件

温度60 °C

反応手順

Bromotrifluoroethylene (41.5 g, 257 mmol) was distilled (dry ice condenser) into a flask containing zinc (13.6 g, 208 mmol) and N,N-dimethylformamide (153 ml), and the resulting mixture was heated at approximately 60° C. for two hours. The reaction mixture was purged with nitrogen for one hour, cooled to −8° C., treated with cuprous bromide (29.83 g, 208 mmol), and stirred for 30 minutes without external cooling. 3-(4-chlorophenyl)-3-bromopropyl methyl ether (17.06 g, 64.7 mmol) in N,N-dimethylformamide (10 ml) was added followed by limonene (5 drops), and the resulting mixture was heated at 50° C. for 8 hours. The cooled reaction mixture was quenched with aqueous ammonium chloride and thoroughly extracted with hexane. The combined organic extracts were dried over anhydrous sodium sulfate and concentrated in vacuo to a brown oil (10.76 g). Chromatography on silica gel eluting with methylene chloride:hexane (1:9) afforded the title compound as a yellow oil (2.25 g), which was characterized by IR, 1HNMR and mass spectral analysis.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06506800B2
出典データセットuspto-grants-2003_01
ORD IDord-e561f314e7744366a11168dbac168c4f
出典メモuspto-grants-2003_01