介绍了加氢法制备邻氯苯胺小试、中试的过程。
The procedure of lab-scale test and pilot experiment of o-aminochlorobenzene preparation by hydrogen process were introduced.
与氯苯胺有关的最重要的反应之一是土壤成分的结合。
One of the most important reactions involving chloroanilines is binding of soil components.
逆流解离萃取通过套用萃取酸分离间氯苯胺及对氯苯胺。
The separation ofm-chloroaniline and p-chloroaniline was carried out by countercurrent dissociation extraction(CDE).
迄今为止的研究报道表明，对氯苯胺的生物降解只能以邻位途径或修饰邻位途径进行。
Up to date, p-chloroaniline was reported to be biodegraded only through ortho-or modified ortho-cleavage pathway.
方法用钒酸氧化法测定血清总胆红素，并与二氯苯胺法和改良J - G法测定结果比较。
Methods Vanadate oxidation of serum total bilirubin, and dichloroaniline law and the law of JG improved results.
空气中三氯苯胺用50％乙醇吸收，经OV-17和OV-210混合色谱柱分离，电子捕获检测器检测测定。
Trichloroaniline in the air was collected with 50% ethanol and separated with a column OV 17:OV 210 ECD as a detector.
空气中三氯苯胺用微孔滤膜采集，环已烷解吸，经OV- 17和OV- 2 10混合色谱柱分离，电子捕获检测器检测测定。
Trichloroaniline in the air was collected with micropore filter membrane and desorbed with cyclohexane, separated with a column OV-17:OV-210 and determined by GC-ECD.
以2,3 -二氯苯胺为原料，经3步亲核取代反应合成了阿立哌唑。3步反应的收率分别为83%，91%和90%；总收率68%。
Aripiprazole in overall yield of 68% was synthesized from 2, 3-dichloroaniline by a three-step nucleophilic substitution reaction in yield of 83%, 91% and 90%, respectively.
测定了降解途径中相关酶的活性，表明对氯苯胺经过苯胺双加氧酶初始氧化和羟基化后，芳环的裂解是由邻苯二酚2 ，3双加氧酶催化。
Enzymatic analysis show that initial reactions ofp-chloroaniline degradation by Diaphorobacter sp. PCA039 are catalyzed by aniline dioxygenase and chlorocatechol 2,3-dioxygenase.
本文以邻甲基苯胺、对氯苯胺、间三氟甲基苯胺和5-三氟甲基-1，3-苯二胺为单体，利用电化学方法，得到了上述苯胺衍生物的聚合物薄膜。
In this paper, polymer films were prepared with o-toluidine, p-chloroaniline, m-trifluoro methylaniline and 5-trifluoromethyl-1,3-diaminobenzene as monomer by electrochemical method.
以2-氰基-4-硝基苯胺为原料，用直接卤化法研制成2-氰基-4-硝基-6-氯苯胺、2-氰基-4-硝基-6-溴苯胺、和2-氰基-4-硝基-6-碘苯胺。
With 2-cyano-4-nitro-aniline as raw material, 2-cyano-4-nitro-6-halogen- anilines have been prepared by direct halogenation.
将七号位碳上的溴基取代成各种苯胺类衍生 物，再与4-甲氧基-磺基氯苯反应得到6-氮基吲哚-1-磺胺。
The 7-bromo group was replaced with various aniline, and then treated with 4- methoxybenzenesulfonyl chloride to afford the 6-azaindole-1-sulfonamides.
将七号位碳上的溴基取代成各种苯胺类衍生 物，再与4-甲氧基-磺基氯苯反应得到6-氮基吲哚-1-磺胺。
The 7-bromo group was replaced with various aniline, and then treated with 4- methoxybenzenesulfonyl chloride to afford the 6-azaindole-1-sulfonamides.
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