Reacción #10373

Ecuación de reacción

hydrochloric acid

2,4,5-Trifluoro-3-formylbenzoic acid

triethylamine

O-benzylhydroxylamine hydrochloride

→

3-(benzyloxyiminomethyl)-2,4,5-trifluorobenzoic acid

Rendimiento 100.0%

Disolventes

tetrahydrofuran

brine

Condiciones de reacción

Tratamiento posterior

1. 1
   ExtracciónThe mixture is extracted with ethyl acetate
2. 2
   SecadoThe organic phase is dried over Na2SO4
3. 3
   Filtraciónfiltered
4. 4
   Concentraciónconcentrated in vacuo

Procedimiento

2,4,5-Trifluoro-3-formylbenzoic acid (Horiuchi N., Yonezawa T., Chiba K., Yoshida H., PCT Int. Appl. [1999] WO 97-JP2918), (5.70 g, 27.9 mmol), triethylamine (11 mL, 78.9 mmol), O-benzylhydroxylamine hydrochloride (4.47 g, 28.0 mmol) and anhydrous tetrahydrofuran (150 mL) are stirred at room temperature for 50 hours. The mixture is poured into brine and the pH adjusted to 5.5–6.0 using 1.0 M hydrochloric acid. The mixture is extracted with ethyl acetate. The organic phase is dried over Na2SO4, filtered, and concentrated in vacuo to provide 3-(benzyloxyiminomethyl)-2,4,5-trifluorobenzoic acid (8.63 g), which is used without further purification. 1H NMR (200 MHz, CDCl3): δ 9.82–9.18 (bs, 1H), 8.24 (s, 1H), 7.94–7.68 (m, 1H), 7.55–7.23 (m, 5H), 5.23 (d, 2H). MS (EI, M−1) m/z 308.

Fuente