Reaktion #54180
ord-172d9fc38690431cb00e89f3fd122624
Reaktionsgleichung
HCl
ethyl cyanoacetate
aldehyde
6-Hydroxy-7-methoxy-5-benzofurancarboxaldehyde
sodium hydroxide
→
7-Oxo-9-methoxy-7H-furo[3,2-g][1]benzopyran-6-carboxylic acid
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1workup.ADDITIONthen treated with 8 ml
- 2TemperaturAfter cooling
- 3Sonstigethe product was isolated by centrifugation
- 4Sonstigefollowed by crystallization from ethanol
- 5Sonstigeto yield a yellow solid, m.p. 227°-228°
Vorschrift
The aldehyde of Example 5 (192 mg., 1 mmole) in 1 ml. of water was added to a solution of ethyl cyanoacetate (125 mg., 1.1 mmole) in 1 ml. of water containing 200 mg. of sodium hydroxide. The mixture was stirred at room temperature for 20 hours then treated with 8 ml. of 2N HCl under reflux for 30 minutes. After cooling, the product was isolated by centrifugation followed by crystallization from ethanol to yield a yellow solid, m.p. 227°-228°.