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3-METHOXY-4-(2-PIPERIDIN-1-YL-ETHOXY)-BENZALDEHYDE synthesis

5synthesis methods
-

Yield:46995-88-4 91.07 %

Reaction Conditions:

with tetrabutylammomium bromide;potassium carbonate;potassium iodide in acetonitrile;

Steps:

4.1.5. General method of obtaining intermediates 7a-7d (method B)

General procedure: 3-Hydroxy-4-methoxybenzaldehyde (1 eq), K2CO3 (1 eq), KI (0.1 eq),the corresponding small molecule amine (2 eq) were dissolved in anhydrous acetonitrile. The mixture was stirred for 11 h at refllux. The reaction mixture was quenched with water (30.00 mL) and extracted with EtOAc (3 × 40.00 mL). The organic phases were combined, dried over Na2SO4, filtered and concentrated under reduced pressure to provide product.

References:

Xu, Huashen;Wang, Jianmin;Chen, Yuanguang;Du, Yang;Chen, Lu;Wu, Chunfu;Wang, Lihui;Chen, Guoliang [European Journal of Medicinal Chemistry,2023,vol. 250,art. no. 115171]