تفاعل #2122483

معادلة التفاعل

(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

المذيبات

THF

THF

ظروف التفاعل

المعالجة

1. 1
   أخرىThe suspension obtained
2. 2
   درجة الحرارةrefluxed under argon for one hour
3. 3
   درجة الحرارةAfter cooling to room temperature
4. 4
   تركيزthe reaction mixture was concentrated
5. 5
   workup.ADDITIONwater was added
6. 6
   استخلاصThe aqueous layer was extracted with dichloromethane
7. 7
   غسيلthe combined organic layers were then washed with brine
8. 8
   تجفيفdried over sodium sulfate
9. 9
   ترشيحAfter filtration and concentration under vacuum
10. 10
    أخرىthe residue was purified by column chromatography (silica gel, ethyl acetate 100%)

الإجراء التجريبي

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.

المصدر