二乙胺

The better reaction conditions of the way are as follows: Reaction temperature is 75C ; The ratio of cyanamide to diethylamineis 1:2.0; Reaction time is 5 hour.

该合成工艺较优的反应条件是，反应温度75℃，氰胺与二乙胺的投料比为1：2.0，反应时间5小时。

Over the AlPO〓, the deamination and dealkylation of diethylmine and triethylmine produced ethylene selectivily. Over AlPONs of acid-base bifunctional catalysts the ethylnitrol formed selectivily.

二乙胺、三乙胺在酸性的磷酸铝上选择性的脱烷基/脱氨生成乙烯，在酸碱两性的氮化磷酸铝上选择性脱烷基/脱氢生成乙腈。

The deoiling effect of the polymerized additives has been evaluated by means of aerated floatation process.The result shows that when dimethylamine,diethylamine or methylamine serves as amine and the molar ratio of ...

利用充气浮选法对所合成的药剂进行了除油效果的评价，结果表明：当胺为二甲胺、二乙胺、甲胺，聚合单体与环氧氯丙烷的摩尔比为1：2时，产品的除油效果最佳。

Take CdS for account, hexagonal spherical CdS with average particle size of 50nm was formed in pyridine, cubic rod-like in 1,6 hexyl diamine, mixtures of cubic and hexagonal spherical particles in biethylamine .

以CdS为例，在吡啶中形成六方相球形CdS纳米晶，平均粒径约为50nm；在1-6已二胺中得到的是棒状立方纤锌矿的CdS；在二乙胺中，得到的是立方和六方的混合相，产物形貌为球形粒子。

Goal compound synthesis namely: Take the vanillic acid as outset raw material, obtains 4- hydroxyl - 3- anisole methyl formate with the methyl alcohol reflux conditions, then after the etherification, the nitration, the return to original state, the ring closure response obtains 6- methoxy - 7- animal pen oxygen radical kui zuo lin - 4- alkone, then passes through the chlorination, the substitution aniline, to escape responses again and so on animal pen oxygen radical, etherification to obtain the goal compound; The goal compound and the diethylamine had the amine substitution reaction to obtain TM1, namely 4- benzene amino - 6- methoxy - 7- [2- hydroxyl - 3-(N, N- two ethyl aminos) third oxygen radical] kui zuo lin; Through zuo has the etherification with the Austria niter to respond obtains TM2, namely 4- benzene amino - 6- methoxy - 7- [2- hydroxyl - 3-(2- methyl - 5- nitryl imidazole) third oxygen radical] kui zuo lin.

目标化合物的合成即：以香草酸为起始原料，与甲醇回流条件下得到4-羟基-3-甲氧基苯甲酸甲酯，然后经过醚化、硝化、还原、环合反应得到6-甲氧基-7-苄氧基喹唑啉-4-酮，然后再经氯化、取代苯胺、脱苄氧基、醚化等反应得到目标化合物；目标化合物与二乙胺发生胺取代反应得到了TM1，即4-苯氨基-6-甲氧基-7-[2-羟基-3-丙氧基]喹唑啉；通过与奥硝唑发生醚化反应得到TM2，即4-苯氨基-6-甲氧基-7-[2-羟基-3-(2-甲基-5-硝基咪唑)丙氧基]喹唑啉。

Synthesis of target compounds namely: to vanillic acid as the starting material with methanol under reflux conditions for 4 - hydroxy -3 - p-methyl, then ether, and nitration, reduction, cyclization reaction 6 - methoxy -7 - benzyloxy-quinazoline -4 - one, and then by the chloride in place of aniline, benzyloxy-off, such as etherification reaction of the target compounds; target compounds with the second and third occurrence of substitution reactions of amines by the TM1, that is, 4 - amino-benzene -6 - methoxy -7 - [2 - hydroxy -3 -(N, N-diethyl amino) oxy c] quinazoline; with ether occurred Ornidazole reaction of TM2, namely, 4 - amino-benzene -6 - methoxy -7 - [2 - hydroxy -3 -(2 - methyl -5 - nitroimidazole) C oxy] quinazoline.

本论文以嘌呤类似物喹唑啉为母核，分别在其4位和7位引入结构多样的取代苯氨基和柔性侧链，设计了一系列4-取代苯胺基-6-甲氧基-7-(2-羟基取代丙氧基)喹唑啉类化合物。目标化合物的合成即：以香草酸为起始原料，与甲醇回流条件下得到4-羟基-3-甲氧基苯甲酸甲酯，然后经过醚化、硝化、还原、环合反应得到6-甲氧基-7-苄氧基喹唑啉-4-酮，然后再经氯化、取代苯胺、脱苄氧基、醚化等反应得到目标化合物；目标化合物与二乙胺发生胺取代反应得到了TM1，即4-苯氨基-6-甲氧基-7-[2-羟基-3-丙氧基]喹唑啉；通过与奥硝唑发生醚化反应得到TM2，即4-苯氨基-6-甲氧基-7-[2-羟基-3-(2-甲基-5-硝基咪唑)丙氧基]喹唑啉。

Methods The effects of different concentrations of diethylamine on the permeation of glibenclamide from emulgel through rat skin were investigated using vertical diffusion cells.

采用改进的Franz扩散池，考察不同浓度二乙胺、不同有机胺和促进剂对格列本脲透皮吸收的影响，并评价优选处方对正常大鼠的降血糖作用。

N,N-diethylaminopropylmethyldimethoxysilane was synthesized by taking γ-chloropropylmethyldimethoxysilane and diethylamine as raw materials in the process of amination .

以γ -氯丙基甲基二甲氧基硅烷和二乙胺为原料，经过胺化反应制得N N -二乙基-氨丙基甲基二甲氧基硅烷。

At room temperature, solution's pH=11, mole proportion of solution are 1:3 (ammonium sulfate and diethyl amine),1 :2.5(ammonium sulfate and diethylene triamine) and 1:2 (ammonium sulfate and triethylene tetramine).

在室温下，固定剂溶液pH=11，溶液物质的量配比分别为硫酸铵与二乙胺1：3、硫酸铵与二乙烯三胺1：2.5和硫酸铵与三乙烯四胺1：2。

The results showed: when TLC solvent system was: chloroform - methanol - diethyl amine = 90:9:1, alkaloids from lotus leaves were well isolated, and five components were isolated and identified by spraying Dragendorff reagent. The optimal conditions of HPLC solvent system were: methanol- water - diethyl amine = 75:25:0.0125. Under the conditions, components of alkaloids from lotus leaves were separated very well, and ideal RP-HPLC peaks were obtained.5、Methods of High Speed Counter Current Chromatography and preparative High Performance Liquid Chromatography applied to identify and purify alkaloids from lotus leaves were set up. When solvent system of HSCCC was: chloroform - methanol - water (pH=4.00)= 4:3:2, speed of chromatogram was 700rpm, flow speed of the mobile phase was 2mL/min, four pure components relatively were attained by isolation and purification.

结果表明：薄层层析溶剂系统为氯仿：甲醇：二乙胺=90：9：1，使荷叶中的生物碱达到了较好的分离效果，并用改良的碘化铋钾试剂喷雾显色，共分离鉴别出了5种荷叶生物碱；分析型HPLC分析检测的较优溶剂系统为甲醇：水：二乙胺=75：25：0.0125，使荷叶生物碱的各个组分达到了基线分离，并获得了较好的峰形。5、建立了高速逆流色谱和制备型HPLC技术分离纯化荷叶生物碱的具体方法。H(来源：ABC46论文网www.abclunwen.com)SCCC法在溶剂系统为氯仿：甲醇：pH4.00的水=4：3：2，色谱仪转速为700rpm，流动相流速为2mL／min的条件下，分离纯化得到了4个纯度较高的化合物。

According to the clear water experiment, aeration performance of the new equipment is good with high total oxygen transfer coefficient and oxygen utilization ratio.

曝气设备的动力效率在叶轮转速为120rpm～150rpm时取得最大值，此时氧利用率和充氧能力也具有较高值。

The environmental stability of that world - including its crushing pressures and icy darkness - means that some of its most famous inhabitants have survived for eons as evolutionary throwbacks, their bodies undergoing little change.

稳定的海底环境─包括能把人压扁的压力和冰冷的黑暗─意谓海底某些最知名的栖居生物已以演化返祖的样态活了万世，形体几无变化。