制备了用对硝基苯甲酰氯处理的间氯甲酚或3-羟基-4-氯苯酚，并转化为取代的对硝基苯甲酮。
M-chlorocresol or 3-hydroxy-4-chlorophenol on treatment with p-nitrobenzoyl chloride was prepared and conyerted into substituted p-nitrobezyl ketone.
以二苯醚与苯甲酰氯为原料，合成了一种新型的激光光敏刺——4 -苯氧基二苯甲酮(PBZP)。
A new photoinitiator, 4-phenoxy benzophenone (PBZP), was synthesized and characterized using diphenyl ether and benzoyl chloride as raw material.
它主要由苯甲酰氯和苯酚制备苯甲酸苯酯，然后重排、醚化所得。
It is based on phenol benzoate which is made from benzoyl chloride and phenol through rearrangement and etherification.
以过氧化二苯甲酰（BPO）为引发剂，在1 ，2 -二氯乙烷溶液中进行了丙烯酸接枝ABS树脂。
The graft copolymerization of acrylic acid onto acrylonitrile butadiene styrene(ABS) terpolymer was initiated by benzoyl peroxide (BPO) in 1,2 dichloroethane solution.
综述了苯甲酰异氰酸酯的合成路线，并探讨了利用苯甲酰胺与草酰氯制备苯甲酰异氰酸酯的最佳反应条件。
Preparation methods of benzoyl cyanate were reviewed. The optimal conditions of synthesis of benzoyl cyanate from benzoyl amine and oxalyl chloride were investigated.
以苯甲酰氯为原料，经酰化，还原，环合等反应合成左旋西替利嗪盐酸盐，反应总收率为8.05%。
Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation, hydrogenation, cyclization with an overall yield of 8.05%.
以苯甲酰氯为原料，经酰化，还原，环合等反应合成左旋西替利嗪盐酸盐，反应总收率为8。05%。
Levocetirizine dihydrochloride was prepared from benzoyl chloride by acids lation hydrogenation cyclization with an overall yield of8.05%.
本课题以二茂铁为原料，与邻甲氧基苯甲酰氯反应生成邻甲氧基苯甲酰基二茂铁，再与一系列胺反应合成亚胺，最终还原为二茂铁氨基化合物。
The title compounds were obtained by the reduction of the corresponding ferrocenyl imines, which were prepared from ferrocene and o-anisic acid chloride, followed by amination with aromatic amines.
叙述了苯甲酰氯的性质、合成工艺路线、实验室和工业制法，产品规格及其分析方法。并对其深加工产品及其应用进行了概述。
In this paper the synthetic methods and properties of benzoyl chloride are introduced, and its downstream products and its application are stated.
本文报道了以邻氯甲苯为原料，经光氯化、水解、取代三步合成2-甲酰基苯磺酸钠的方法，并对影响反应收率的因素进行了讨论。
Sodium 2-formylbenzenesulfonate was prepared from 2-chlorotoluene by photo-chlorination, hydrolysis and substitution reactions successively. Factors affecting the yields were discussed.
给出了二氯苯膦直接氧化合成苯膦酰二氯的方法。
In this paper, A new and simple synthetic method of phenylphosphonic dichloride from direct oxidation of dichlorophenylphosphine was described.
由苯与异丁酰氯在无水三氯化铝作催化剂的条件下制备苯基异丙基酮。
Methyl 1 phenyl Propanone was synthesized with benzene and iso butyryl chloride by using anhydrous aluminium trichloride as catalyst.
方法以对硝基苯甲酰氯为起始原料，经缩合、还原、重氮化、偶合、成盐等反应制得巴柳氮二钠。
METHODS Balsalazide disodium was synthesized by reactions of condensation , reduction, diazotization , coupling and salification from 4-nitrobenzoyl chloride.
改进了中间体3，5-二硝基-4-二正丙胺基苯磺酰氯和最终产品安磺灵的合成方法，使之更适合于工业生产的要求。
The syntheses of 3,5-dinitro-4-di-n-propylamidobenzenesulfong chloride and oryzalin was improved, makes more is fit for the requirement in the industrial production.
苯甲酰氯和d酒石酸反应生成d 2, 3二苯甲酰酒石酸酐，后者于丙酮水溶液中水解得到拆分剂d 2, 3二苯甲酰酒石酸。
The resolving reagent, D-2, 3-dibenzoyl tartaric acid was obtained by hydrolyzation of D-2, 3-dibenzoyl tartaric anhydride prepared by reaction of benzoyl chloride with D-tartaric acid.
方法：以对硝基苯甲酰氯为原料，经氨解、氢化、重氮化及偶合四步反应得到了巴柳氮。
METHODS:This compound was synthesize by steps of ammonolysis, hydrogenize, diazotization and coupling from 4 nitrobenzoyl chloride.
以二氧杂环己烷为溶剂，通过聚乙二醇2 70与对甲基苯磺酰氯反应合成了1 8冠6，产率64 .4 %。
Also, in dioxane solution, 18Crown6 was prepared in 64.4% yields by reaction of polyethylene glycol 270 and ptoluenesulfonyl chloride.
以二氧杂环己烷为溶剂，通过聚乙二醇2 70与对甲基苯磺酰氯反应合成了1 8冠6，产率64 .4 %。
Also, in dioxane solution, 18Crown6 was prepared in 64.4% yields by reaction of polyethylene glycol 270 and ptoluenesulfonyl chloride.
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