Reaktion #215764

Reaktionsgleichung

lithium hydroxide

lithium hydroxide

Methyl 2-methoxy-4-(1-Boc-4-piperidyloxy)benzoate

→

2-methoxy-4-(1-Boc-4-piperidyloxy)benzoic acid

Lösungsmittel

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONadded over 5 min
2. 2
   Temperaturthe mixture was heated
3. 3
   Temperaturat reflux for 13 hours
4. 4
   workup.STIRRINGstirred at ambient temperature for 18 hours
5. 5
   EinengenThe reaction mixture was concentrated in vacuo
6. 6
   Sonstigethe residue partitioned between ethyl acetate and 1N hydrochloric acid
7. 7
   WaschenThe organic layer was washed with brine
8. 8
   Trocknendried over sodium sulfate
9. 9
   Filtrationfiltered
10. 10
    Sonstigeevaporated to dryness in vacuo

Vorschrift

Methyl 2-methoxy-4-(1-Boc-4-piperidyloxy)benzoate (4.5 g, 12.3 mmol) was dissolved in THF (200 ml) and treated with a solution of lithium hydroxide (17 ml of a 1.1M aqueous solution, 18.7 mmol) added over 5 min. The mixture was stirred at ambient temperature for 72 hours. An additional 4 ml of 1.1M lithium hydroxide was added and the mixture was heated at reflux for 13 hours, then stirred at ambient temperature for 18 hours. The reaction mixture was concentrated in vacuo and the residue partitioned between ethyl acetate and 1N hydrochloric acid. The organic layer was washed with brine, dried over sodium sulfate, filtered, and evaporated to dryness in vacuo to give 2-methoxy-4-(1-Boc-4-piperidyloxy)benzoic acid.

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