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HRID 919166作成日:2026年10月25日

Triethylamine → 2-Fluoro-4-(trifluoromethyl)aniline

https://huagongshe.com/reaction/919166

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物2-Fluoro-4-(trifluoromethyl)benzoic acidHCID 518003—
触媒Cuprous chlorideHCID 62652—
溶媒tert-ButanolHCID 6386—
生成物2-Fluoro-4-(trifluoromethyl)anilineHCID 273767458%

反応条件

温度50 °C

反応手順

To the solution of 2-fluoro-4-(trifluoromethyl)benzoic acid (1 kg, 4.805 mol, 1.00 equivalent “eq.”) and CuCl (14.26 g, 0.144 mol, 0.03 eq.) in t-BuOH (11.7 L) was added triethylamine (TEA, 533.8 g, 5.286 mol, 1.10 eq.) dropwise at room temperature (rt). Then the solution was heated to 50° C. and diphenylphosphoryl azide (DPPA, 1393 g, 5.045 mol, 1.05 eq.) was added dropwise to the solution at 50-60° C. After heating at 80˜85° C. overnight the solution was concentrated under vacuum. The residual was dissolved in H2O and filtered. The filtrate was extracted with ethyl acetate. The organic layers was dried with Na2SO4, filtered and concentrated under vacuum. The residual was dissolved in tert-Butyl methyl ether (TBME) and HCl (gas) was bubbled in for 2 hours. The filtrate was collected and dissolved in water and basified with 2 M NaOH. The solution was extracted with TBME. The organic layers were dried and concentrated under vacuum to give 2-fluoro-4-(trifluoromethyl) aniline (498 g, 58%) as a red oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09273007B2
出典データセットuspto-grants-2016_03
ORD IDord-d935a6917e6944fb8540c86ba1aaf421
出典メモuspto-grants-2016_03