Реакция #2122483

Уравнение реакции

(2,4,5-trimethyl-phenyl)acetic acid methyl ester

4-hydroxy-1-methoxy-piperidine-4-carboxylic acid ethyl ester

potassium tert-butoxide

→

4-Hydroxy-8-methoxy-3-(2,4,5-trimethyl-phenyl)-1-oxa-8-aza-spiro[4.5]dec-3-en-2-one

Растворители

THF

THF

Условия реакции

Обработка

1. 1
   ДругоеThe suspension obtained
2. 2
   Температураrefluxed under argon for one hour
3. 3
   ТемператураAfter cooling to room temperature
4. 4
   Концентрированиеthe reaction mixture was concentrated
5. 5
   workup.ADDITIONwater was added
6. 6
   ЭкстракцияThe aqueous layer was extracted with dichloromethane
7. 7
   Промывкаthe combined organic layers were then washed with brine
8. 8
   Сушкаdried over sodium sulfate
9. 9
   ФильтрацияAfter filtration and concentration under vacuum
10. 10
    Другоеthe residue was purified by column chromatography (silica gel, ethyl acetate 100%)

Методика

To a solution of (2,4,5-trimethyl-phenyl)acetic acid methyl ester (0.6 g, 3.12 mmol) and 4-hydroxy-1-methoxy-piperidine-4-carboxylic acid ethyl ester (0.76 g, 3.74 mmol) in 7 ml anhydrous THF was added a 1 M solution of potassium tert-butoxide (6.9 ml, 8.87 mmol) in THF at room temperature. The suspension obtained was first stirred at room temperature for one hour, and then refluxed under argon for one hour. After cooling to room temperature, the reaction mixture was concentrated, water was added and the mixture acidified with little HCl (37%). The aqueous layer was extracted with dichloromethane, and the combined organic layers were then washed with brine and dried over sodium sulfate. After filtration and concentration under vacuum, the residue was purified by column chromatography (silica gel, ethyl acetate 100%). Yield: 280 mg of 4-hydroxy-8-methoxy-3-(2,4,5-trimethyl-phenyl)-1-oxa-8-aza-spiro[4.5]dec-3-en-2-one (title compound P2.2) as a white solid, mp 199-204° C.

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