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西藏麝香合成新工艺 被引量:1

A new Process for Synthesis of Musk Tibetene
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摘要 以催化重整C9芳烃分离装置分离出均三甲苯、偏三甲苯后的副产品重组分溶剂(169~178℃馏分)—混合C9芳烃为原料,其中含连三甲苯40%~50%,以三氯化铝为催化剂与异丁烯进行烷基化反应,合成出5 叔丁基 1,2,3 三甲基苯中间体,经蒸馏后,用混酸进行硝化反应得到西藏麝香。本方法不但具有工艺路线简单,生产成本低的特点,同时也解决了富集连三甲苯的利用问题。 In this process , the heavy fraction solvent (169~178℃)— mixed C_(9) aromatic hydrocarbon, namely, the by-product of mesitylene and pseudocumene which were separated from C_(9) aromatic hydrocarbon catalytic reforming separation facility , will be the feedstock which was alkylated by isobutene in presence of aluminium trichloride as catalyst to synthesize 5-tert-butyl-1,2,3 trimethyl benzene intermediate product which , after distillation ,was nitrated with nitro-sulfuric acid to obtain Musk Tibetene. This method is low cost and simple in design , and the pregnant hemimellitene is fully used in this process.
出处 《精细化工中间体》 CAS 2004年第6期37-38,61,共3页 Fine Chemical Intermediates
关键词 西藏麝香 C9芳烃 异丁烯 Musk Tibetene C_(9) aromatic hydrocarbon isobutene
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参考文献4

  • 1何坚 孙宝国.香料化学与工艺学[M].北京:化学工业出版社,1995.221-222.
  • 2张承曾 汪清如.日用调香术[M].北京:中国轻工业出版社,1993..
  • 3Laura M. Matz, Pete S. Tornatore, Herbert H. Hill Evaluation of suspected interferents for TNT detection by ion mobility spectrometry[J]. Talanta ,2001, 54:171~179
  • 4DeRidder, Dirk J. A.; Schenk, Henk crystal studies of musk compoundsXIV. a redetermination of the molecular structures of three nitrobenzene musks: discussinon of the geometer of a tert-butyl group attached to a benzene ring and embedded by two nitro groups Bull. Soc. Chim. Belg. 1995,104(2) :81~96.

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  • 1何坚 孙宝国.香料化学与工艺学[M].北京:化学工业出版社,1995.221-222.

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