A one-pot green synthesis of 1,3-oxazinan-2-ones from amines and 1,3-diols in the presence of a dialkyl carbonate and potassium tert-butoxide is described. Four dialkyl carbonates were utilised: dimethyl carbonate, diethyl carbonate, diprop-2yl carbonate and tert-butyl methyl carbonate. The more hindered the dialkyl carbonate used, the higher the yield of 1,3-oxazinan-2-one. Four 1,3-diols were reacted having primary-primary, primary-secondary, primary-tertiary and secondary-tertiary functionalities, with the yield of oxazinanone decreasing with increasing hindrance of the diol. In the case of the diols containing primary and either secondary or tertiary functionality, the substituent(s) were selectively found in the 6 position of the so-formed oxazinanone. The best found conditions were then employed with different nucleophiles i.e., phenylhydrazine, aniline and n-octylamine.

1,3-Oxazinan-2-ones from amines and 1,3-diols through dialkyl carbonate chemistry

ARICO', Fabio;TUNDO, Pietro
2012

Abstract

A one-pot green synthesis of 1,3-oxazinan-2-ones from amines and 1,3-diols in the presence of a dialkyl carbonate and potassium tert-butoxide is described. Four dialkyl carbonates were utilised: dimethyl carbonate, diethyl carbonate, diprop-2yl carbonate and tert-butyl methyl carbonate. The more hindered the dialkyl carbonate used, the higher the yield of 1,3-oxazinan-2-one. Four 1,3-diols were reacted having primary-primary, primary-secondary, primary-tertiary and secondary-tertiary functionalities, with the yield of oxazinanone decreasing with increasing hindrance of the diol. In the case of the diols containing primary and either secondary or tertiary functionality, the substituent(s) were selectively found in the 6 position of the so-formed oxazinanone. The best found conditions were then employed with different nucleophiles i.e., phenylhydrazine, aniline and n-octylamine.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/10278/34421
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