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Treatment of dials with N-tert-butanesulfinamide, all biaryl dials were successfully converted into the corresponding bis-imines which were then treated with samarium diiodide to afford diamine products. The absolute configurations of all the intramolecular coupling products were determined by X-ray crystallography.

轴手性二醛与N-叔丁基亚磺酰胺缩合得到相应的亚胺,其为一对非对映异构体。N-叔丁基亚磺酰亚胺在二碘化钐条件下得到的偶联产物,经X-衍射也确定了其立体构型。

Tetrachloroterephthalic acid was prepared by chlorinating terephthalic acid, oleumsolvent and iodine catalyst. Tetrachloroterephthalic acid was acylated by sulphurous oxychloride in the presence of DMF to form tetrachloroterephthaloyl chloride. The acyl chloride product was fluorinated by potassium fluoride and esterified by methanol to synthesize dimethyl tetrafluoroterephthalate. The ester was reduced with potassium borohydride and lithium chloride to give tetrafluoroterephthalyl alcohol. The above product was bromated in the hydrobromic acid to obtain 4-bromomethyl-2,3,5,6-tetrafluoro-benzene methanol. 4-Methyl-2,3,5,-6-tetrafluorobenzene ethanol was obtained by reducing the bromide with magnesium. In the exist of DCC and DMAP, tefluthrin was got by the condensation reaction between 4-methyl-2,3,5,6-tetrafluoro-benzene methanol and-(1RS,3RS)- 3-(2- chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethyl cycolpropanecar-boxylate acid.

对苯二甲酸与氯气在碘存在下以发烟硫酸为溶剂进行氯化制备四氯对苯二甲酸;再以DMF为催化剂与二氯亚砜反应生成四氯对苯二甲酰氯;以氟化钾为氟化剂,环丁砜为溶剂置换氟化,再与甲醇酯化得到四氟对苯二甲酸甲酯;以KBH4-LiCl为还原剂二甲醚为溶剂反应制得四氟对苯二甲基苄醇;以氯苯为溶剂在溴化氢溶液中溴化得到溴化产物;在乙醇溶液中经镁粉还原得到4-甲基-2,3,5,6-四氟苄醇;甲基苄醇与功夫酸在催化剂二环己基碳二亚胺和4-二甲氨基吡啶作用下缩合得到七氟菊酯,总收率达43.6%。

The final product Rimonbant was then obtained in 64% yield via chlorination of the acid with oxalyl chloride followed by treatment of the resultant acyl chloride with 1-aminoperidine.

氯与1-氨啶在三乙胺存在下缩合生成目标产物利莫那班,产率64%。

The final product Rimonbant was then obtained in 64% yield via chlorination of the acid with oxalyl chloride followed by treatment of the resultant acyl chloride with 1-aminoperidine.

酰氯与1-氨哌啶在三乙胺存在下缩合生成目标产物利莫那班,产率64%。

In the same reactor, telon fast green 5G was synthesized through condensation and sulfonation processes with 1,4,5,8-hydroxyanthraquinone and p-toluidine as main raw materials.

由1,4,5,8—四羟基蒽醌和对甲苯胺为主要原料,在一个反应器内同时完成了缩合和磺化两步单元反应,合成酸性蒽醌绿染料,并对其反应条件对产物收率的影响进行了研究,确定了最佳合成工艺条件(反应时间16 h、反应温度120℃、原料的配比1:2.2)。

The similar nicotinoyltrifluoroacetones are synthesized from acetylpyridine and ethyl trifluoroacetate through Claisen reaction.The influnences of alcoholic natrium,reaction temperature and solvent on reaction yield is studied.The subliming method is improved.

本文以乙酰吡啶和三氟乙酸乙酯为主要原料,利用克莱森酯缩合反应,合成了三种相似结构的吡啶甲酰三氟丙酮化合物,考察了碱性试剂醇钠、反应温度和溶剂等因素对反应产率的影响,改进了纯化产物的方法。

The synthesis of alkylcyclohexylbenzoic acid: take the synthesis of ethylcyclohexylbenzoic acid as a typical example. With the AlCl3 as the catalyst, cis+trans acetylcyclohexylbenzene is synthesized from the reaction of acetyl chloride, cyclohexene and benzene.

烷基环己基苯甲酸的合成研究:主要研究了乙基环己基苯甲酸的合成,以乙酰氯、环己烯、苯为原料,三氯化铝为催化剂,合成乙酰基环己基苯,用水合肼、氢氧化钾、一缩二乙二醇经过高温加热还原羰基(Wolff-黄鸣龙还原),将所得到的乙基环己基苯用乙酰氯进行傅克酰基化得到乙基环己基苯乙酮,所得中间体经过处理之后直接得到反式产物,将反式异构体的乙酰基氧化得到反式烷基环己基苯甲酸。

Especially it introduces the parameter of the cross aldol condensation and side-reaction controlling, the midterm products separation, and catalyzed hydrogenation.

重点研究了交叉缩合及副反应的控制、中间产物脱水及催化加氢的有关参数。

This paper mainly studies the synthesis of 2-Isopropyl-5-Methyl-2-Hexenal from the optimum reaction conditions of from self aldol condensation of Isovaleraldehy,with NaOH solution as the catalyst of the condensation.

本文以NaOH水溶液为催化剂,探讨了异戊醛Aldol缩合制备可可醛(2异丙基5甲基2己烯醛)的最佳反应条件:反应温度50℃、反应时间9h、催化剂NaOH水溶液的浓度2mol.L1、OH-/异戊醛为1/1,主产物可可醛的产率为92.2%。

The primary content of this paper is the synthesis of POSS with r-glycidyl-propyl-trimethoxysilane throught hydrolysis and condensation reaction and the modification of shape memory polyurethane with synthesized POSS.

本文主要研究了以γ-(2,3环氧丙氧)丙基三甲氧基硅烷为原料通过水解缩合反应合成含有羟基的POSS以及利用该产物改性形状记忆聚氨酯。

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