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1.The optimum preparation technology was conducted by orthogonal design L9(34) with different ratios on yield of product. The initial conditions of synthesizing technology were determined: in acid making, n -butanol and 2-ethyl-hexanol:phosphorus pentasulfide = 4.2∶1 ,the charging temperature was 60 ℃ . reaction temperature was 95 ℃ , reaction time was 1.5 h;
制酸阶段与成盐阶段都采用4因素3水平进行正交实验,通过因素时收率影响的分析,得出制备ZDDP最佳工艺条件为:制酸阶段,醇与五硫化二的摩尔比为4.2∶1,加料温度为60℃,反应温度为95℃,反应时间为1.5 h;收藏指正
2.The selective thionation of α acetylamino β [4(1,2 dihydro 2 oxoquinoline)]propionic acid and its ester with phosphorus pentasulfide as a thionation reagent yielded the target compound α acetylamino β [4(1,2 dihydro 2 thioquinoline)]propionate. The structure of the new compound was studied by IR、UV、+ 13 C NMR、GC/MS and Element analysis,and substitutional site of thionation of acetylamine was discussed.
:α 乙酰氨基 β [4 (1,2 二氢 2 氧代喹啉 ) ]丙酸乙酯以五硫化二为硫化剂 ,经选择性硫代反应合成新化合物α 乙酰氨基 β [4 (1,2 二氢 2 硫代喹啉 ) ]丙酸乙酯 ,并使用IR、UV、NMR、GC/MS及元素分析对其结构进行了鉴定收藏指正
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