Issue 25, 2013

Lactam/MoCl5 interaction in CH2Cl2: synthesis and X-ray characterization of protonated δ-valerolactam salts

Abstract

The protonated lactam salts Image ID:c3ra23305g-u1.gif, 1, Image ID:c3ra23305g-u2.gif, 2, and Image ID:c3ra23305g-u3.gif, 3, were isolated from the non selective reaction of MoCl5 with δ-valerolactam in dichloromethane, carried out with different molar ratios. The 1 : 2 reaction of MoCl5 with N-methyl-2-pyrrolidone afforded the chloroiminium salt Image ID:c3ra23305g-u4.gif, 4, in 74% yield, together with minor amount of Image ID:c3ra23305g-u5.gif, 5. The products 1–5 were characterized by analytical and spectroscopic techniques, and by X-ray diffractometry in the cases of 1 and 3.

Graphical abstract: Lactam/MoCl5 interaction in CH2Cl2: synthesis and X-ray characterization of protonated δ-valerolactam salts

Supplementary files

Article information

Article type
Paper
Submitted
12 Dec 2012
Accepted
28 Mar 2013
First published
22 May 2013

RSC Adv., 2013,3, 10007-10013

Lactam/MoCl5 interaction in CH2Cl2: synthesis and X-ray characterization of protonated δ-valerolactam salts

F. Marchetti, G. Pampaloni and S. Zacchini, RSC Adv., 2013, 3, 10007 DOI: 10.1039/C3RA23305G

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