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1125-96-8

2-(3-Pyridinyl)-2-pyrroline synthesis

3synthesis methods
2-Pyrrolidinone, 1-(1-buten-1-yl)-3-(3-pyridinylcarbonyl)-

1308392-26-8
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Yield:1125-96-8 82%

Reaction Conditions:

with nitric acid at 5; for 8 h;Reagent/catalyst;

Steps:

3 Example 3

Add 150g of sodium ethoxide and 1000mL of methyl tert-butyl ether into a three-necked flask, install the magnet and condenser, and replace the system with nitrogen; replace 100g of methyl nicotinate and 117g of N-butenylpyrrolidone with 200mL of methyl tert-butyl ether the base is evenly mixed, the system is slowly heated to 50°C, and the mixed solution is added dropwise. After dropping, the reaction is kept for 3 hours, and then cooled to 5°C. 6N (ie: 6mol/L) nitric acid is added dropwise to quench the reaction and adjust the pH value. React for 8 hours until 4; add at the end of the reaction6N lye adjustmentWhen the pH value reached 10, dichloromethane was added for extraction three times; the organic phases were combined, dried, concentrated, and distilled to obtain 9.233 g of the light yellow oily enamine intermediate with a yield of 82%.

References:

CN112745294,2021,A Location in patent:Paragraph 0044-0045