Reacción #91020

Ecuación de reacción

tert-butyl 4-(3,5-dichloro-4-ethoxybenzamido)-2-methoxybenzoate

tert-Butyl 4-(3,5-dichloro-4-ethoxybenzamido)-2-methoxybenzoate

boron trichloride

water

NaHCO3

→

4-(3,5-dichloro-4-ethoxybenzamido)-2-hydroxybenzoic acid

Rendimiento 24.0%

Disolventes

DCM

DCM

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.WAITat RT for 2 h
2. 2
   TemperaturaThe reaction mixture was cooled to 0° C.
3. 3
   FiltraciónThe resulting white precipitate was collected by filtration
4. 4
   Lavadowashed with water (2 mL)
5. 5
   OtroThe solid was dried
6. 6
   Otropurified by capture and release on SAX
7. 7
   Lavadoeluting with 5% AcOH in THF

Procedimiento

A solution of tert-butyl 4-(3,5-dichloro-4-ethoxybenzamido)-2-methoxybenzoate (5) (55 mg, 0.13 mmol) in DCM (5 mL) was cooled to 0° C. and treated dropwise with a solution of 1 M boron trichloride in DCM (349 μL, 349 μmol). The reaction mixture was stirred at 0° C. for 1 h and then at RT for 2 h. The reaction mixture was cooled to 0° C. and water (0.5 mL) and sat. aq. NaHCO3 (2 mL) were added. The resulting white precipitate was collected by filtration and washed with water (2 mL). The solid was dried, then purified by capture and release on SAX, eluting with 5% AcOH in THF to afford 4-(3,5-dichloro-4-ethoxybenzamido)-2-hydroxybenzoic acid (AAA-057) (11 mg, 24%) as a white solid: m/z 370 [M+H]+ (ES+), 368 [M−H]− (ES−); 1H-NMR (400 MHz, DMSO-d6) δ: 10.51 (1H, s), 8.06 (2H, s), 7.76 (1H, d), 7.48 (1H, d), 7.28 (1H, dd), 4.14 (2H, q), 1.91 (1H, s), 1.40 (3H, t), 1.35 (1H, s).

Fuente