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N-Anisoyl-4-piperidone synthesis

6synthesis methods
-

Yield:91586-26-4 82.2%

Reaction Conditions:

with triethylamine in dichloromethane at 25; for 1 h;

Steps:

6.2 Preparation of 1-(4-methoxybenzoyl)piperidin-4-one

4-Methoxybenzoyl chloride (1.6 g, 9.4 moles)Dissolved in dichloromethane (15 mL),Ice bath, add triethylamine (1.018,1011111101)And 4-4-piperidone(0.998,1011111101),Rise to room temperature (25 ° (:) reaction for one hourAfter completion of the reaction, 100 mL of dichloromethane was added and the mixture was washed with 100 mL of water. The organic phase was dried over anhydrous sodium sulfate and concentrated. The product 1.818 was isolated by column chromatography (PE: ETA = 5: 1) in 82.2% yield.

References:

CN107226808,2017,A Location in patent:Paragraph 0238; 0242-0244