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呱西替柳合成方法的改进 被引量:1

A Modified Synthesis of Guacetisal
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摘要 本文介绍了在三氯化磷存在下,水杨酸与愈创木酚作用生成水杨酸愈创木酚酯的方法,产物用异丙醇重结晶,收率为75.4%.所得产物再用吡啶作催化剂进行乙酰化,得到呱西替柳,收率为96~97%. A improvement of synthetic method of which guaiacol salicylate was pro-duced by using salicylic acid and guaiacol as starting material under the condition of phosphorus trichlororide was suggested in this paper. The obtained ratio of the prod-ucts recrystalled from isopropanol is about 75.4%. The products derived from the last preparation was acetylated by using pyridine as a catalyst, guacetisal was obtained finally. The obtained ratio of guacetisal is 96-97%.
出处 《黑龙江大学自然科学学报》 CAS 1993年第1期91-93,共3页 Journal of Natural Science of Heilongjiang University
关键词 酯化 三氯化磷 吡啶 呱西替柳 : Esterification Phosphorus trichloride Pyridine Guacetisal
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参考文献2

  • 1孙长安,黄建军.呱西替柳的合成[J].中国医药工业杂志,1990,21(9):387-388. 被引量:7
  • 2刘钊杰,胡汉斌,张景龄.脲系磷化合物的研究(Ⅳ)——O-乙基-O-芳基-硫代磷酰硫脲的研究[J]华中师范大学学报(自然科学版),1987(03).

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  • 1吴洋,艾军,张淑梅,王云普.引发剂“PV”的合成[J]化学试剂,1985(04).

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