论文部分内容阅读
The reaction of naphthalene with oxalyl chloride in the presence of anhydrous AlCl 3 was investigated. The homolog of dinaphthyl methanone can be obtained mainly from this reaction. Naphthalene conversion does not have evident correlation with the amount of AlCl 3. The results show that the reaction proceeds via carbon cation electrophilic substitution reaction free radical substitution reaction pathway.
The reaction of naphthalene with oxalyl chloride in the presence of anhydrous AlCl 3 was investigated. The homolog of dinaphthyl conversion can be obtained mainly from this reaction. Naphthalene conversion does not have evident correlation with the amount of AlCl 3. The results show that the reaction disposed via carbon cation electrophilic substitution reaction free radical substitution reaction pathway.