ChloromethacrylonitrileおよびChloroisobutyronitrileに関する研究(第3報)ChloromethacrylonitrileおよびChloroisobutyronitrileのエーテル化合物への誘導
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Substitution reactions of chloroisobutyronitriles and chloromethacrylonitriles with sodium methoxide in methanol were studied. The reaction products were isolated by fractional distillation or gas chromatography and their structures confirmed. The main products were saturated ether compounds, i. e., β-methoxyisobutyronitriles, but small quantities of unsaturated ethers, i. e., methoxymethacrylonitriles, were formed in certain cases. 2-Chloromethyl-2,3-dichloropropionitrile (7), and trans-and cis-3-chloro-2-chloromethyl-acrylonitriles (5a, 5b) gave a common end product, 2-dimethoxymethyl-3-methoxypropionitrile (15), but gave different reaction intermediates. Methyl 2-chloromethyl-2,3-dichloropropionimidate (18) was obtained from 7 and 2-dimethoxymethylacrylonitrile (16) from 5a and 5b.
- 公益社団法人日本薬学会の論文
- 1973-10-25
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関連論文
- ChloromethacrylonitrileおよびChloroisobutyronitrileに関する研究(第3報)ChloromethacrylonitrileおよびChloroisobutyronitrileのエーテル化合物への誘導
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