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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 35, 2005 - Issue 16
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Original Articles

Acylation Studies with Meldrum's Acid

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Pages 2139-2141 | Received 05 Feb 2005, Published online: 18 Aug 2006
 

Abstract

Meldrum's acid (1) on bisacylation with succinyl chloride afforded a neutral diketo product (2); however, the dimer enolic products (3) with acidic nature resulted in glutaryl and adipyl dichlorides. Monoacylation of (1) with acetyl chloride gave acidic 5‐acetyl Meldrum's acid (4) in enol form.

Presented at the National Symposium on Newer Concepts in Organic Synthesis, 1998, Aurangabad, India, [Abstract: 1.29].

This paper is dedicated to Prof. M. M. Salunkhe, Vice-Chancellor, Shivaji University, Kolhapur–416 004 (Former Director, Institute of Science, Mumbai – 400 032) India.

Acknowledgment

We thank the University Grants Commission, New Delhi, India, for financial assistance.

Notes

Presented at the National Symposium on Newer Concepts in Organic Synthesis, 1998, Aurangabad, India, [Abstract: 1.29].

This paper is dedicated to Prof. M. M. Salunkhe, Vice-Chancellor, Shivaji University, Kolhapur–416 004 (Former Director, Institute of Science, Mumbai – 400 032) India.

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