Reacción #302846

Ecuación de reacción

hydrochloric acid

5′-bromo-2′-hydroxyacetophenone

compound 1

5′-bromo-2′-hydroxyacetophenone

4-nitrobenzoyl chloride

→

compound 2

4-nitrobenzoic acid 2-acetyl-4-bromophenyl ester

Disolventes

pyridine

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe obtained mixture was reacted at room temperature for 30 minutes
2. 2
   Temperaturaunder cooling on ice
3. 3
   FiltraciónThe obtained precipitate was collected by filtration
4. 4
   Lavadothe filtrate was then washed with purified water

Procedimiento

5′-bromo-2′-hydroxyacetophenone (compound 1) (863 mg, 4.65 mmol) was added to a pyridine solution (20 ml) that contained 4-nitrobenzoyl chloride (1.00 g, 4.65 mmol) in an ice bath. The obtained mixture was reacted at room temperature for 30 minutes, and the reaction solution was then poured into 1 N hydrochloric acid under cooling on ice. The obtained mixture was intensively stirred. The obtained precipitate was collected by filtration, and the filtrate was then washed with purified water, so as to obtain a product of interest, 4-nitrobenzoic acid 2-acetyl-4-bromophenyl ester (compound 2). Yield: 1.57 g (yield constant: 92.7%) 1H NMR (300 MHz, CDCl3) δ 8.37 (s, 4H), 8.00 (s, 1H), 7.76-7.72 (m, 1H), 7.16 (d, J=8.7 Hz, 1H), 2.55 (s, 3H). MS m/z 365 (MH+).

Fuente