Enantioselective hydrogenation of α,β-unsaturated carboxylic acids in fixed-bed reactor

Autor:	Beáta Hermán, Mihály Bartók, Ferenc Fülöp, György Szőllősi
Rok vydání:	2007
Předmět:	chemistry.chemical_classification Process Chemistry and Technology Carboxylic acid Enantioselective synthesis chemistry.chemical_element Heterogeneous catalysis Catalysis Solvent chemistry.chemical_compound Benzylamine chemistry Organic chemistry Cinchonidine Palladium
Zdroj:	Applied Catalysis A: General. 331:39-43
ISSN:	0926-860X
DOI:	10.1016/j.apcata.2007.07.022
Popis:	The enantioselective hydrogenation of four α,β-unsaturated carboxylic acids has been studied over cinchona alkaloid-modified supported Pd catalyst in a high-pressure continuous-flow system using a fixed-bed reactor. The hydrogenation of the aliphatic substrates resulted in products of slightly lower enantioselectivities as obtained in batch reactors under similar reaction conditions. The optical purity of the product formed in the hydrogenation of α-phenylcinnamic acid was over 70%, exceeding the values obtained in slurry reactor in the same solvent. It was shown that the enantioselectivity increasing effect of benzylamine is kept in the fixed-bed reactor. Based on the results obtained by changing the modifier concentration in the feed we suggest that the interaction of the substrates with cinchonidine may occur in the liquid phase and the complex formed is adsorbed on the Pd surface. Thus, relatively high concentration of such complex and consequently modifier amount is necessary for obtaining good enantioselectivities in the hydrogenation of α,β-unsaturated carboxylic acids.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::c9b907117ceab6989dbc4244cb00757b https://doi.org/10.1016/j.apcata.2007.07.022 Zobrazit plný text záznamu Full Text from ScienceDirect