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Synthesis 2013; 45(17): 2481-2484
DOI: 10.1055/s-0033-1338504
DOI: 10.1055/s-0033-1338504
paper
Study of the Kulinkovich Synthesis of 1-Methylcyclopropanol and Its Conversion into 1-Methylcyclopropyl 4-Nitrophenyl Carbonate
Further Information
Publication History
Received: 20 April 2013
Accepted after revision: 17 June 2013
Publication Date:
26 July 2013 (online)
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Abstract
A detailed investigation of the preparation of 1-methylcyclopropanol via the Kulinkovich reaction is presented. Reaction and workup parameters were optimized to provide a reproducible procedure for the synthesis of multigram quantities of 1-methylcyclopropanol. Key improvements were the use of titanium tetra(2-ethyl)hexyloxide as catalyst, reduction in the volume of reaction solvent, addition of the methyl acetate starting material in portions, and azeotropic distillation to remove by-products. The preparation of the 4-nitrophenyl carbonate ester was likewise studied and optimized.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis. Included are the experimental procedure and 1H NMR spectra of the NMR study of the conversion of 1 into 2 mediated by pyridine and triethylamine and notes on the origin of by-products in the Kulinkovich reaction.
- Supporting Information
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References
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See, for example:
Other methods have been reported to produce 1; however, these methods appear to have limited preparative value and remain as isolated instances of the preparation of 1, see: