N-乙烯基咔唑的合成及表征  被引量:1

Synthesis and Characterization of N-vinyl Carbazole

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作  者:许浩然[1] 王海洋[1] 王广兴[1] 金丹[1] 姜辉[1] 赵巍[1] 王艳慧 张亮亮 XU Hao-ran;WANG Hai-yang;WANG Guang-xing;JIN Dan;JIANG Hui;ZHAO Wei;WANG Yan-hui;ZHANG Liang-liang(Sinostccl An sha n Research In stitute of Thermo-energy Co.,Ltd.,Anshan 10041,China)

机构地区:[1]中钢集团鞍山热能研究院有限公司,鞍山10041

出  处:《当代化工》2022年第4期800-804,共5页Contemporary Chemical Industry

基  金:辽宁省企业技术创新重点项目,电子级N-乙烯基咔唑研发及产业化(项目编号:20V787)。

摘  要:以咔唑和甲基丁炔醇为原料,反应生成N-乙烯基咔唑,反应液经过进一步处理得到纯品N-乙烯基咔唑。考察了反应用溶剂、反应温度及反应时间对N-乙烯基咔唑收率的影响。结果表明:合成产物的最佳溶剂是DMSO,最佳反应温度为140℃,最佳反应时间为12 h。产物经FTIR、^(1)HNMR、^(13)CNMR进行结构表征。N-乙烯基咔唑的液相色谱纯度>99.5%,气相色谱纯度>99.5%,熔点64℃,总产率85%,合成产物可作为电子级化学品使用。N-vinyl carbazole was produced by reaction from carbazole and methyl butanediol, and the pure N-vinyl carbazole was obtained by further treatment of reaction liquid.The effects of reaction solvent, reaction temperature and reaction time on the yield of N-vinyl carbazole were investigated. The results showed that the best solvent for the synthetic product was DMSO, the best reaction temperature was 150 ℃, and the best reaction time was 12 h. The structure of the product was characterized by FTIR, ^(1)H NMR and ^(13)CNMR.The liquid chromatography purity of n-vinyl carbazole was >99.5%, the gas chromatography purity was > 99.5%, the melting point was 64 ℃, the total yield was 85 %, the synthetic products can be used as electronic grade chemicals.

关 键 词:咔唑 甲基丁炔醇 DMSO N-乙烯基咔唑 电子级化学品 

分 类 号:TQ251.35[化学工程—有机化工]

 

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