Sodium Hydroxide → Benzofuran-7-Carboxylic Acid
Reaktionsgleichung
[O:1]1[C:5]2[C:6]([C:10]([O:12]C)=[O:11])=[CH:7][CH:8]=[CH:9][C:4]=2[CH:3]=[CH:2]1.[OH-].[Na+]>CO>[O:1]1[C:5]2[C:6]([C:10]([OH:12])=[O:11])=[CH:7][CH:8]=[CH:9][C:4]=2[CH:3]=[CH:2]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
(1)-(i) A mixture of 420 mg of methyl benzofuran-7-carboxylate, 5 ml of an aqueous 10% sodium hydroxide solution and 5 ml of methanol is stirred at room temperature for 1 hour. The reaction mixture is evaporated to remove solvent. The residue is dissolved in water and the solution is acidified with 10% hydrochloric acid. The resultant crystals are collected by filtration and dried to give 321 mg of benzofuran-7-carboxylic acid as colorless crystals.
Aufarbeitung
- customThe reaction mixture is evaporated
- customto remove solvent
- dissolutionThe residue is dissolved in water
- filtrationThe resultant crystals are collected by filtration
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-ee157fa10fc94d07a242545f44bb72fa
- Quelldatensatz
- uspto-grants-1989_05
- Patentnummer
- US04829067
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