Reaktion #302857

Reaktionsgleichung

5′-methoxy-2′-hydroxyacetophenone

4-nitrobenzoyl chloride

hydrochloric acid

→

compound 21

4-nitrobenzoic acid 2-acetyl-4-methoxyphenyl ester

Lösungsmittel

pyridine

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe obtained mixture was reacted at room temperature for 30 minutes
2. 2
   Temperaturunder cooling on ice
3. 3
   FiltrationThe obtained precipitate was collected by filtration
4. 4
   Waschenthe filtrate was then washed with purified water

Vorschrift

5′-methoxy-2′-hydroxyacetophenone (1.5 g, 9.03 mmol) was added to a pyridine solution (20 ml) that contained 4-nitrobenzoyl chloride (1.72 g, 9.26 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-methoxyphenyl ester (compound 21). Yield: 2.49 g (yield constant: 87.4%)

Quelle