Summary
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1
A study was made of the conditions under which carbon tertrachloride reacts with phenyl vinyl, butyl vinyl, and ethyl ethers in presence of benzoyl peroxide.
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2.
It was found that, in presence of benzoyl peroxide, vinyl ethers are able to react with carbon tetrachloride with formation of both equimolecular-addition products and polymetric products, depending on the original proportions of reactants.
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3.
The characteristics of the resulting phenyl, ethyl, and butyl 1,3,3,3-tetrachloropyl ethers were determined. Their hydrolytic decomposition was studied, and it was shown that, in the case of the phenyl ether, it can provide a quantitative method for the determination of the concentration of the ether.
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4.
The mobility of α-chloro in the 1,3,3,3-tetrachloropyl ethers was demonstrated in hydrolytic-scission reactions and in the exchange reaction with an alcohol.
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5.
The polymeric products form by addition of carbon tetrachloride to phenyl vinyl, ethyl vinyl, and butyl vinyl ethers were isolated and characterized.
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Shostakovsky, M.F., Bogdanova, A.V., Zverov, M.M. et al. Oligomerization. Russ Chem Bull 5, 1263–1268 (1956). https://doi.org/10.1007/BF01173785
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DOI: https://doi.org/10.1007/BF01173785