Réaction #51609
ord-b6e11d698b0b4e43a46330c8a8509f06
Équation de réaction
Réactifs
Réactifs
Aucun
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Températurerefluxed for 2 hours
- 2AutreThe solvent was evaporated
- 3workup.ADDITIONThe residue was added to a mixture of acetic acid (150 ml) and hydrochloric acid (50 ml)
- 4workup.STIRRINGThe reaction mixture was stirred
- 5Températurerefluxed for 1 hour
- 6workup.ADDITIONThe mixture was poured out onto ice
- 7FiltrationThe resulting precipitate was filtered off
- 8Autredried (vacuum; 70° C.)
Mode opératoire
A mixture of 1-[2-hydroxy-3-methyl-4-(phenylmethoxy)phenyl]-ethanone (0.098 mol) and ethanedioic acid, diethyl ester (0.11 mol) in toluene (100 ml) was added dropwise to a mixture of sodium methoxide (0.22 mol) in toluene (150 ml). The reaction mixture was stirred and refluxed for 2 hours. The solvent was evaporated. The residue was added to a mixture of acetic acid (150 ml) and hydrochloric acid (50 ml). The reaction mixture was stirred and refluxed for 1 hour. The mixture was poured out onto ice. The resulting precipitate was filtered off and dried (vacuum; 70° C.), yielding 29 g (95.4%) of 8-methyl-4-oxo-7-(phenylmethoxy)-4H-1-benzopyran-2-carboxylic acid (interm. 9).