Reaktion #410058
ord-3ba37cce7b7d4a3497a10cae57bd6450
Reaktionsgleichung
3-benzyloxyphenol
ethyl (RS)-4-chloro-4-phenylbutanoate
potassium carbonate
potassium iodide
→
ethyl (RS)-4-(3-benzyloxyphenoxy)-4-phenylbutanoate
Ausbeute 17.1%
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturis heated
- 2Temperaturat reflux for 40 hours
- 3SonstigeThe mixture is evaporated to dryness
- 4Sonstigethe residue is partitioned between ethyl acetate (200 mL) and water (200 mL)
- 5TrocknenThe organic layer is dried over magnesium sulphate
- 6Filtrationfiltered
- 7Einengenconcentrated in vacuo
- 8WaschenFlash chromatography of the resulting oil, eluting with a mixture of ethyl acetate and cyclohexane (1:19 v/v)
Vorschrift
A mixture of 3-benzyloxyphenol (3 g), ethyl (RS)-4-chloro-4-phenylbutanoate (4.53 g), potassium carbonate (4.14 g), potassium iodide (100 mg) and methyl ethyl ketone (100 mL) is heated at reflux for 40 hours. The mixture is evaporated to dryness and the residue is partitioned between ethyl acetate (200 mL) and water (200 mL). The organic layer is dried over magnesium sulphate, filtered, and concentrated in vacuo. Flash chromatography of the resulting oil, eluting with a mixture of ethyl acetate and cyclohexane (1:19 v/v), gives ethyl (RS)-4-(3-benzyloxyphenoxy)-4-phenylbutanoate (1 g), in the form of a yellow oil.