Sodium Hydroxide → 7-Chloro-1-benzothiophene-2-carboxylic acid
Reaktionsgleichung
[Cl:1][C:2]1[C:7]2[S:8][C:9]([C:11]([O:13]C)=[O:12])=[CH:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>C(O)C>[Cl:1][C:2]1[C:7]2[S:8][C:9]([C:11]([OH:13])=[O:12])=[CH:10][C:6]=2[CH:5]=[CH:4][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Methyl 7-chlorobenzo[b]thiophene-2-carboxylate (3 g, 13 mmol) was dissolved is ethanol (15 mL) and treated 5 N sodium hydroxide (5 mL). The reaction was heated at reflux overnight. The volatiles were removed in vacuo and the aqueous residue was acidified to pH 2 using 5 N HCl. The resulting white solid was filtered off, washed well with water and dried in a vacuum oven at 60° C. Yield=2.6 g. MS (M−H)− 210.
Aufarbeitung
- temperatureThe reaction was heated
- temperatureat reflux overnight
- customThe volatiles were removed in vacuo
- filtrationThe resulting white solid was filtered off
- washwashed well with water
- customdried in a vacuum oven at 60° C
Quellen und Nachweise
- ORD-Eintrag
- ord-fea189dc2932427e8c75b27d77b41223
- Quelldatensatz
- uspto-grants-2010_08
- Patentnummer
- US07786132B2
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