苯酰胺

The optimum reaction conditions are as follows: diphenylmethanethiol : methyl chloroacetate is 1:1.5, and the reaction carried out at 100℃ for 4 h, 2- acetamide can be carried out in the room temperature for 20 h, the yield of 2- acetamide was 76%, hydrogen dioxide: 2- acetamide is 1:1, and the reaction carried out at 60℃ for 3 h, the yield of modafinil was 79%, the total yield of reaction can be reached 48%.

研究表明，采用氯乙酸甲酯作为醚化试剂，反应时间4h，反应温度100℃，二苯甲硫醇：氯乙酸甲酯=1：1.5，室温下氨解反应20h，二苯甲硫乙酰胺收率76%；采用过氧化氢作为氧化试剂，反应时间3h，反应温度60℃，过氧化氢：二苯甲硫乙酰胺=1：l，莫达非尼收率79%，反应总收率可达48%。

Experimental solubilities of terephthalic acid dissolved in N,N-dimethyl propionamide, N,N-diethyl propionamide and N,N-diethyl acetamide were determined in the temperature range of

测定了303.2~363.2K温度范围内，对苯二甲酸在N，N-二甲基丙酰胺、N，N-二乙基丙酰胺和N，N-二乙基乙酰胺中的溶解度。

Methods 4-Hydroxy- benzonitrile was treated with sodium hydrogen sulfide and anhydrous magnesium chloride in dimethyl formamide to give thioamide, which was then directly cyclized with ethyl 2-chloroacetoacetate without separation to give ethyl 2-(4-hydroxyphenyl)-4-methylthiazole-5-carboxylate(2) in one-pot; then 2 was formylated with Duff reaction adopting hexamethylenetetramine in trifluoroacetic acid to give ethyl 2-(3-formyl-4-hydroxyphenyl)-4-methylthiazole-5-carboxylate(3); finally, the target compound was obtained by the treatment of 3 with hydroxylamine hydrochloride and sodium formate in formic acid.

采用"一勺烩"方法，以4-羟基苯甲腈为起始原料，首先与硫氢化钠和无水氯化镁在N，N-二甲基甲酰胺中反应，所得中间体不经分离，直接加入2-氯乙酰乙酸乙酯进行环合反应，得到2-(4-羟基)苯基-4-甲基-5-噻唑甲酸乙酯（2）；然后通过六亚甲基四胺/三氟乙酸进行Duff反应，得到2-(3-甲酰基-4-羟基)苯基-4-甲基-5-噻唑甲酸乙酯（3）；再经盐酸羟胺/甲酸/甲酸钠体系脱水得到目标化合物。

Two classes of specific binding sites in the polymer matrix were investigated by Scatchard analysis, which indicated that two kinds of complexes between functional monomers and templates were formed before the polymerization process. Comparing with the structure of TNT and acrylamide, one kind of complex between TNT and acrylamide was strongly charge-transfer complexing interaction by p-πcomplex between electron-rich amino group of acrylamide and electron-deficiecy-benzene ring of TNT, the other was hydrogen bonding interaction between amino group (-NH_2) of acrylamide molecule nitro group (-NO_2) of TNT.

Scatchard分析结果表明，在TNT印记聚合物微球中存在两类结合位点，这表明在聚合反应之前，TNT与功能单体丙烯酰胺分子之间存在两种不同类型的作用力而自组装成两类的模板分子-功能单体复合物，一类可能是由于富电子的丙烯酰胺和缺电子的TNT的苯环通过p-π配键而形成的电荷转移复合物，另一类可能是由于丙烯酰胺的胺基与TNT的硝基之间的氢键作用而形成的复合物。

A series of 2-oxocyclododecyl sulfonylurea s have been synthesized from 2-oxocyclododecylsulfonamide via acylation of phenyl chloroformate and amination.

以环十二酮为起始原料，经磺化反应制备得到2-氧代环十二烷基磺酸盐B，B经过氯化和胺解反应制备得到2-氧代环十二烷基磺酰胺C，C经过苯氧酰化与胺解反应后合成了10个新的2-氧代环十二烷基磺酰脲类化合物D，它们的结构通过了1HNMR和IR的确证。

Gemini surfactant, sodium oleoylamidodiphenyl ether disulfonate was synthesized from p-nitrodiphenylether,oleoyl choride and chlorosulphonic acid through nitro-group reduction,acylation and sulphonation.

以对硝基二苯醚、油酸酰氯、氯磺酸为主要原料，通过硝基还原反应、胺基酰化反应、磺化反应，合成了双子表面活性剂油酸酰胺基二苯醚双磺酸钠；并用IR，1HNMR，MS对产品及中间体结构进行了表征。

A process for preparingp-fluo-2-(2-methyl-3-propionyl)-4-oxy-N,3-diphenyl-phenylbutylamide includes such steps as Friedle-Craft acylating of newly prepared phenylacetyl chloride and fluorobenzene under catalysis of AlCl3 to obtain 4-fluoro-phenylbenzyl ketone, brominating at carbonyl alpha position under catalysis of less AlCl3 to obtain alpha-bromo-4-fluo-phenylbenzyl ketone, and condensing with isobutyryl acetanilide under action of sodium ethoxide.

本发明涉及一种制备对氟－2－(2－甲基－3－氧丙基)－4－氧－N，3－二苯基－苯丁酰胺(1)的方法，其包括以下步骤：新制的苯乙酰氯与氟苯在AlCl3催化下进行Friedle－Craft酰化反应，得到对4－氟－苯基苄基酮(4)；化合物(4)在少量AlCl3催化下进行羰基α位溴化，得到α－溴－4－氟－苯基苄基酮(5)；然后(3)异丁酰乙酰苯胺在乙醇钠作用下与化合物(5)进行缩合。

Cellulose benzoate,the degree of substitution of which was calculated from the content of C determined by element analysis,was prepared from microcrystalline celluloseand benzoyl chloride under heterogeneous condition and characterized by FT-IR and~1H-NMR.

研究了微晶纤维素和苯甲酰氯在多相条件下合成制备纤维素苯甲酸酯的反应，通过元素分析所得碳的质量百分含量计算了产物的取代度，并系统研究了吡啶与N，N-二甲基乙酰胺或与三乙胺混合反应溶剂、苯甲酰氯与纤维素羟基的摩尔比r、反应温度和反应时间对D S的影响，用FT-IR和1H-NM R对产物进行了表征。

The company developed dmmer acid synthesis technology in Sichuan bentonite mainly catalyst,the product quality and finished product rate both were much better than the internal industry(dimmer acid color:≤7#,viscosity:between 5000~10000cp/250C adjustable,finished product rate:≥10% internal industry);a series products project:dimer acid、monomer acid、benzene dissolved polyamide resin、alcohol dissolved polyamine resin and polyamine hotmelt adhesive,let enterprises in the fierce market competition,flexible adjustment product structure,to cope with the market with facility.

公司研发的以四川膨润土为主催化剂的二聚酸合成技术，在产品质量和产品收率上均大大优于国内同行业（二聚酸色泽≤7#，粘度在5000～10000cp/250C之间可调，收率高于同行业10%）；系列化的产品方案：二聚酸、单体酸、苯溶聚酰胺树脂、醇溶聚酰胺树脂、液体聚酰胺树脂及聚酰胺热溶胶，让企业在激烈的市场竞争中，灵活调整产品结构，做到应对市场游刃有余。

The company developeddmmer acid synthesis technology in Sichuan bentonite mainly catalyst , the product quality and finished product rate both were much better than the internal industry(dimmer acid color:≤7#, viscosity : between 5000~10000 cp/250C adjustable , finished product rate :≥10% internal industry); a series products project : dimer acid 、 monomer acid 、 benzene dissolved polyamide resin 、 alcohol dissolved polyamine resin and polyamine hotmelt adhesive , let enterprises in the fierce market competition , flexible adjustment product structure , to cope with the market with facility .

本公司自行研发出的以四川膨润土为主催化剂的二聚酸合成技术，在产品质量和产品收率上均大大优于国内同行业产品（二聚酸色泽≤7#，粘度在5000～10000cp/250C之间可调，收率≥10%同行业。）：二聚酸、单体酸、苯溶聚酰胺树脂、醇溶聚酰胺树脂、液体聚酰胺树脂及聚酰胺热溶胶。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。