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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1428997생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1428997

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물2-Fluoro-4-(trifluoromethyl)benzoic acidHCID 518003—
촉매Cuprous chlorideHCID 62652—
용매tert-ButanolHCID 6386—
생성물2-Fluoro-4-(trifluoromethyl)anilineHCID 273767458%

반응 조건

온도50 °C

반응 단계

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 tent-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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08937185B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-7e9b73f7c53c4a14a8f70a7579039688
출처 메모uspto-grants-2015_01