Reaktion #11031

Reaktionsgleichung

chlorosulfonic acid

fumaric acid maleic acid

diethyl 2-(2-nitrophenoxy)fumarate

diethyl 2-(2-nitrophenoxy)maleate

→

8-nitro-2-ethoxycarbonyl-4-oxo-4H-1-benzopyran

Ausbeute 70.0%

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeAfter a reaction container equipped with a stirrer, a cooling tube
2. 2
   workup.ADDITIONwas added dropwise at an inner temperature of 50° C. or below
3. 3
   workup.ADDITIONAfter completion of addition
4. 4
   Sonstigeto obtain a reaction solution

Vorschrift

After a reaction container equipped with a stirrer, a cooling tube and a thermometer was charged with 15 parts by weight of chlorosulfonic acid, 3 parts by weight of a mixture (content: 84.4% by weight, fumaric acid/maleic acid ratio=49/51) containing diethyl 2-(2-nitrophenoxy)fumarate and diethyl 2-(2-nitrophenoxy)maleate was added dropwise at an inner temperature of 50° C. or below. After completion of addition, the inner temperature was raised to 70° C. and the mixture was stirred and kept at the same temperature for 7 hours to obtain a reaction solution containing 8-nitro-2-ethoxycarbonyl-4-oxo-4H-1-benzopyran (reaction yield: 70%). After cooled to room temperature, the reaction solution was gradually added into 24 parts by weight of water. After kept at an inner temperature of 60° C. for 1 hour, the mixture was gradually cooled to an inner temperature of 0° C. Precipitated crystals were filtered and dried to obtain 1.3 parts by weight of a crystalline mixture containing 8-nitro-2-ethoxycarbonyl-4-oxo-4H-1-benzopyran and 8-nitro-2-carboxy-4-oxo-4H-1-benzopyran (the content of 8-nitro-2-ethoxycarbonyl-4-oxo-4H-1-benzopyran: 0.1% by weight; the content of 8-nitro-2-carboxy-4-oxo-4H-1-benzopyran: 86.4% by weight). The yield of 8-nitro-2-ethoxycarbonyl-4-oxo-4H-1-benzopyran was 0.1% and the yield of 8-nitro-2-carboxy-4-oxo-4H-1-benzopyran was 64%.

Quelle