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So the effect of different solvents, such as methanol, ethanol, butanol, tertiary butanol, isoamyl alcohol, tertiary amyl alcohol, diethyl ether and cyclohexane, on the reaction was explored.

在文献所报道的应用K〓CO〓作催化剂、CH〓I既作促进剂又作部分反应物的由原料甲醇与二氧化碳直接合成碳酸二甲酯工作的基础上,在体系中加入离子液体emimBr后,研究了emimBr对合成反应的影响。

This basic research is armed to find out and to predict SCF particularity, which are very important for the SCF application. Firstly the densities of the binary mixtures of CO2—methanol, CO2—ethanol, CO2—n— butyraldehyde and CO2—i—butyraldehyde were measured from 313.5K to 323.5K under the pressure range from 7 to 14MPa.

本文首先在313.5~323.5K、7~14MPa范围内测定了CO2及CO2—甲醇、CO2—乙醇、CO2—正丁醛、CO2—异丁醛二元混合流体的表观密度,讨论了压力、第2组分的种类和加入量对CO2表观密度的影响,在此基础上计算了溶质的偏摩尔体积,讨论了温度、压力和第2组分的性质对溶质偏摩尔体积的影响规律。

The better reaction conditions are as follows: Reaction temperature is 40°C, Reaction time is 5 hour; the ratio of L - phenylalanine to acetic acid and N - formyl - L- aspartyl anhydrideis 1:10.2:1.1, Its yield is 95.4%.

在查阅文献的基础上,得到较优的α-L-天冬氨酰L-苯丙氨酸甲脂盐酸盐的合成方案,在甲醇一水体系中,N-甲酰-α-L-天冬氨酰-L-苯丙氨酸在浓盐酸的作用下60℃水解90分钟,后冷却到15℃加入浓盐酸在20~30℃保温反应96小时,进行甲脂化,形成甲脂盐酸盐,结晶析出。

A preferred form of the invention is a process comprising adding to a quantity of sodium which is covered with a hydrocarbon solvent boiling above 100°C., at least a chemically equivalent proportion of methyl, ethyl or a propyl alcohol, subsequently adding an approximately equivalent proportion of a dialkyl carbonate and of an alkyl phenylacetate, the alkyl groups in these two last-mentioned compounds being preferably the same as the alkyl radical of the above-mentioned lower aliphatic alcohol, heating the mixture to induce reaction and continually distilling out the alcohol formed from the reaction zone.

本发明的理想形式包括下面的工艺过程:把至少处于化学平衡的甲醇,乙醇或丙醇添加到覆盖着沸点超过一百摄氏度的碳氢化合物溶剂中,接着加入大约相同当量的二烷基碳酸酯和烷基乙酸苯酯,在刚才提到的化合物中,其烷基集团最好是和刚才提到的低级别脂肪族醇相同,然后加热反应混合物从而引导反应的进行,在反应区域通过连续蒸馏移除形成的醇类。

Process for the manufacture of a dialkylphenylethylmalonatewhich comprises adding to a quantity of sodium which is covered with a hydrocarbon solvent boiling above 100°C, at least a chemically equivalent proportion of methyl, ethyl or a propyl alcohol, subsequently adding an approximately equivalent proportion of a dialkylcarbonate and of an alkyl phenylacetate, the alkyl groups in these two last-mentioned compounds being preferably the same as the alkyl radical of the above –mentioned lower aliphatic alcohol, heating the mixture to induce reaction and continually distilling out the alcohol formed from the reaction zone and finally causing the sodio diethyl phenylmalonate so formed to interact with an ethylating agent.

生产二烷基苯基丙二酸酯的工艺过程:这包括这包括把至少处于化学平衡的甲醇,乙醇或丙醇添加到覆盖着沸点超过一百摄氏度的碳氢化合物溶剂中,接着加入大约相同当量的二烷基碳酸酯和烷基乙酸苯酯,在刚才提到的化合物中,其烷基集团最好是和刚才提到的低级别脂肪族醇相同,然后加热反应混合物从而引导反应的进行,在反应区域通过连续蒸馏移除形成的醇类。最后使所形成的钠代二乙基苯基丙二酸酯和乙基化试剂反应。

This is the first report of pectenolone and pectenoxanthin, two types of carotenoid, in the muscle of the Yesso scallop.3 Roles of the carotenoids composition and accumulation in Yesso scallopThe method for detecting carotenoids using reverse phase high performance liquid chromatography was developed. The conditions of RP-HPLC analysis were an analytical scale (200×4.6 mm, inner diameter 5μm) Eclipse XDB-C18 column of Agilent corporation; 10μl injection volume; 25°C column temperature; acetonitrile, methanol and methylene dichloride mobile phase (40:56:4, V/VV) with 0.1% BHT; 1.0 ml per minute flow rate; 450 nm UV-VIS detector; 8 minutes elution.The carotenoids from orange muscle of Yesso scallop of 7, 10, 12, 15, 18, 22 months old was detected using the method refered above.

通过柱层析、高效液相等手段对橘红色闭壳肌中的主要类胡萝卜素进行了提取分离,分离提纯得到两种类胡萝卜素,并通过MS、~1H-NMR和~(13)C-NMR对其进行结构鉴定,结果表明(3S,3\'R)-3,3\'-dihydroxy-7\',8\'-didehydro-β,β-Caroten-4-one和(3S,3\'S)-7,7\',8,8\'-tetradehydro-β,β-Carotene-3,3\'-diol,俗称pectenolone和pectenoxanthin是橘红色闭壳肌中的主要类胡萝卜素,这是国内外首次对虾夷扇贝闭壳肌中的类胡萝卜素进行提纯及结构鉴定。3虾夷扇贝类胡萝卜素的种类组成和累积变化规律建立了橘红色闭壳肌中类胡萝卜素的HPLC分析定量检测技术:色普柱为Agilent公司的Eclipse XDB-C18柱200mm×4.6mm,i.d.5μm进样体积,5μl ;流速1ml/min;检测波长450nm;柱温25℃;流动相为乙腈:甲醇:二氯甲烷(V/V/V=40:56:4并加入0.1%的BHT;分离时间为8min。

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