Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.O.[I:10]I.C(=O)(O)[O-].[Na+]>C1COCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([I:10])[CH:3]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 4-chlorophenol in THF (75 mL), and H2O (75 mL) was added a mixture of crushed iodine (78.7 mmol, 20 g) and sodium bicarbonate (78.7 mmol, 6.6 g). The reaction mixture was stirred at room temperature overnight, then quenched with sufficient 5% sodium thiosulfate solution to turn the color of the reaction mixture from deep violet to light yellow and extracted with ether (2×200 mL). The ether layer was collected, washed with H2O, and the washed ether layer was dried, filtered and the filtrate was evaporated to a crude product, which was purified by distillation to obtain 4-chloro-2-iodo phenol (7%, 1.3 g); mp 79° C.-82° C.
Aufarbeitung
- customquenched with sufficient 5% sodium thiosulfate solution
- extractionextracted with ether (2×200 mL)
- customThe ether layer was collected
- washwashed with H2O
- dry with materialthe washed ether layer was dried
- filtrationfiltered
- customthe filtrate was evaporated to a crude product, which
- distillationwas purified by distillation
Quellen und Nachweise
- ORD-Eintrag
- ord-377ea90ca4ef427b88176d5de2f9524e
- Quelldatensatz
- uspto-grants-2005_02
- Patentnummer
- US06849629B2
Verknüpfte Notizen
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