Water → 4-(1h-Benzimidazol-2-yl)benzoic acid
Reaktionsgleichung
[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:19]=[CH:18][C:13]([C:14]([O:16]C)=[O:15])=[CH:12][CH:11]=1.O.[OH-].[Na+]>C1COCC1>[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:19]=[CH:18][C:13]([C:14]([OH:16])=[O:15])=[CH:12][CH:11]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Methyl 4-(1H-benzimidazol-2-yl)benzoate (Step A) (2.63 g) is stirred in THF (50 mL) and water (10 mL) with sodium hydroxide (2.08 g) at reflux for 4 hours. The solvent is evaporated and the residue treated with 2N hydrochloric acid (100 mL). The resulting suspension is collected, washed with methanol/ethyl acetate and dried to give 2.52 g of the title compound as a white solid.
Aufarbeitung
- customThe solvent is evaporated
- additionthe residue treated with 2N hydrochloric acid (100 mL)
- customThe resulting suspension is collected
- washwashed with methanol/ethyl acetate
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-d6321a9b9f97403a91e05f81e8a9d4d6
- Quelldatensatz
- uspto-grants-1996_01
- Patentnummer
- US05486517
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