Reaktion #1917259
ord-90525c054a8648908e59a0cdde8a5e83
Reaktionsgleichung
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1TemperaturThe reaction mixture was heated
- 2Temperaturat reflux for 3 hours
- 3Temperaturcooled
- 4Einengenconcentrated in vacuo
- 5Sonstigeto give an orange oil that
- 6Sonstigewas partitioned between ethyl acetate and 2 N hydrochloric acid
- 7TrocknenThe organic layer was dried over anhydrous sodium sulfate
- 8Filtrationfiltered
- 9Einengenconcentrated in vacuo
Vorschrift
The 4-iodo-2-methoxybenzoic acid methyl ester of Step A (2.7 g, 9.24 mmol) was dissolved in tetrahydrofuran (40 mL) and 1 N sodium hydroxide (20 mL, 20 mmol) was added. The reaction mixture was heated at reflux for 3 hours, then cooled and concentrated in vacuo to give an orange oil that was partitioned between ethyl acetate and 2 N hydrochloric acid. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to give 2.5 g of title product as a yellow-orange solid, m.p. 144–146° C.