Sodium Hydroxide → 4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid
Reaktionsgleichung
[C:1]([C:3]1[C:4]([I:14])=[C:5]([C:10]([O:12]C)=[O:11])[S:6][C:7]=1[S:8][CH3:9])#[N:2].[OH-].[Na+]>O1CCCC1.O>[C:1]([C:3]1[C:4]([I:14])=[C:5]([C:10]([OH:12])=[O:11])[S:6][C:7]=1[S:8][CH3:9])#[N:2]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a solution of methyl 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylate (3.40 g, 10 mmol) in tetrahydrofuran (80 mL) and water (16 mL) was added a solution of 1.00M sodium hydroxide in water (30 mL). The solution was allowed to stir overnight. The reaction was quenched with a solution of 1N hydrogen chloride in water (50 mL) and diluted with water (400 mL). The resultant precipitate was filtered, washed with water (2×100 mL) and dried in a vacuum oven to give 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid (2.6 g, 79%) as a white solid. LCMS: (FA) ES+ 326.
Aufarbeitung
- customThe reaction was quenched with a solution of 1N hydrogen chloride in water (50 mL)
- additiondiluted with water (400 mL)
- filtrationThe resultant precipitate was filtered
- washwashed with water (2×100 mL)
- customdried in a vacuum oven
Quellen und Nachweise
- ORD-Eintrag
- ord-b7f853aa1ac349879e725b4300e7f130
- Quelldatensatz
- uspto-grants-2015_05
- Patentnummer
- US09029411B2
Notizen zur Reaktion
Wird geladen…