Add time:08/24/2019 Source:sciencedirect.com
Carboxylic acids are converted to the corresponding 4-methoxybenzyl (PMB) esters with 4-methoxybenzyl-2,2,2-trichloroacetimidate in the absence of an acid catalyst. This operationally simple procedure is a highly effective method for the formation of PMB esters. The reaction is promoted by the carboxylic acids themselves in excellent yields (72–99%). Sterically hindered carboxylic acids, which provide lower yields with other imidates, are esterified in higher yield with the more reactive PMB imidate. No racemization is observed in the case of carboxylic acids bearing an α-stereocenter, and no isomerization is observed with Z-α,β-unsaturated acids. This method may therefore find use in the esterification of complex or sensitive substrates where more common techniques lead to decomposition.
We also recommend Trading Suppliers and Manufacturers of 2-AMINO-1-(4-METHOXYBENZYL)-4,5,6,7-TETRAHYDRO-1H-INDOLE-3-CARBONITRILE (cas 113772-12-6). Pls Click Website Link as below: cas 113772-12-6 suppliers
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View