Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

57748-41-1

4-(2-PYRIDINYLMETHOXY)BENZALDEHYDE synthesis

5synthesis methods
-

Yield:57748-41-1 88%

Reaction Conditions:

Stage #1: 4-hydroxy-benzaldehydewith potassium carbonate in acetonitrile; for 0.5 h;
Stage #2: 2-chloromethylpyridine in acetonitrile; for 8 h;Reflux;

Steps:

4.2.7 General procedure for the synthesis of benzaldehydes 9a-13a, 9b-13b and 9c-13c

General procedure: The corresponding hydroxybenzaldehyde (1a-1c) was dissolved in dry acetonitrile (15-20mL) and K2CO3 (1.5 eq) was added. The reaction mixture was stirred for 30min and the appropriate halide (1 eq) was added and stirring was continued overnight at reflux temperature. The course of the reaction was monitored by TLC. After completion of the reaction, the solvent was evaporated under reduced pressure and the residue was purified by column chromatography.

References:

Kelly, John M.;Taylor, Martin C.;Baji?, Miroslav;Bokuli?, Ana;Jeli?, Dubravko;Ko?trun, Sanja;Krstulovi?, Luka;Popov, Andrea Bistrovi?;Rai?-Mali?, Silvana;Stojkovi?, Marijana Radi?;Zonji?, Iva [European Journal of Medicinal Chemistry,2020,vol. 207,art. no. 112802]

4-(2-PYRIDINYLMETHOXY)BENZALDEHYDE Related Search: