JOURNAL OF NANJING FORESTRY UNIVERSITY ›› 2004, Vol. 28 ›› Issue (06): 31-34.doi: 10.3969/j.jssn.1000-2006.2004.06.008
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WANG Zong-de~1,XIAO Zhuan-quan~2,CHEN Jin-zhu~1
Online:
Published:
Abstract: Nopol and nopyl ethyl ether were synthesized from β-pinene,and nopyl ethyl ether was oxidized by basic potassium permanganate solution.The results are as follows:(1)The structures of 8 products were identified by GC-MS,they were 2,2-dimethyl-3-(β-ethoxypropionyl)cyclobutanone,cis-2,2-dimethyl-3-(β-ethoxypropionyl) cyclobutaneacetic acid,3-hydroxy-cis-2,2-dimethyl-3-(β-ethoxypropionyl) cyclobutaneacetic acid,1-hydroxy-cis-2,2-dimeth-yl-3-(β-ethoxypropionyl) cyclobutaneacetic acid,2,3-dihydroxy-nopyl ethyl ether,5-hydroxy-2,3-epoxynoyl ethyl ether,1-hydroxy-2,3-epoxynopyl ethyl ether,1,5-dimethyl-2,3-epoxynopyl ethyl ether.(2)Because the isolation of the products was very difficult,so an ester of a main product was isolated through a designed process,and its structure was identified by IR,MS,~1H NMR and~(13)C NMR.It was cis-2,2-dimethyl-3-(β-ethoxypropionyl) cyclobutaneacetate.(3)The results suggested that the first product of this action was 2,3-dihydroxy-nopyl ethyl ether,which could be further cleaved to produce cyclobutaneacetic acid or dehydrated to produce 2,3-epoxide.
CLC Number:
0624.33
TQ351.47+2
WANG Zong-de~1,XIAO Zhuan-quan~2,CHEN Jin-zhu~1. A Study on Oxidation of Nopyl Ethyl Ether[J]. JOURNAL OF NANJING FORESTRY UNIVERSITY, 2004, 28(06): 31-34.
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URL: http://nldxb.njfu.edu.cn/EN/10.3969/j.jssn.1000-2006.2004.06.008
http://nldxb.njfu.edu.cn/EN/Y2004/V28/I06/31