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HRID 50465作成日:2026年10月24日

3-(Trifluoromethoxy)aniline → 3-[(3-Trifluoromethoxyphenyl)amino]-1,1,1-trifluoro-2-propanol

https://huagongshe.com/ja/reaction/50465

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Trifluoromethoxy)anilineHCID 73753—
反応物2-(Trifluoromethyl)oxiraneHCID 520769—
生成物3-[(3-Trifluoromethoxyphenyl)amino]-1,1,1-trifluoro-2-propanolHCID 2350605888.5%

反応条件

温度80 °C

反応手順

EX-321A) 3-Trifluoromethoxyaniline (23.81 g, 134.4 mmol) and 3,3,3-trifluoro-1,2-epoxypropane (3.76 g, 33.6 mmol) were placed into a sealed tube and heated to 80° C. for 24 h. The excess aniline was removed by distillation (70° C. at 16.2 Torr) to give 8.6 g (88%) of the desired 3-[(3-trifluoromethoxyphenyl)amino]-1,1,1-trifluoro-2-propanol product as a light yellow oil. 1H NMR (CDCl3) δ 3.29-3.37 (m, 1H), 3.55 (dd, 1H), 4.20 (m, 1H), 6.48-6.63 (m, 3H), 7.12 (t, 1H). 19F NMR (CDCl3) δ −79.36 (s, 3F), −58.44 (s, 3F).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710089B2
出典データセットuspto-grants-2004_03
ORD IDord-125831f355404da4928ba4be3cf1b344
出典メモuspto-grants-2004_03