β-(2-hydroxy-4-chloro-3-quinolyl)propiolactone

2,4-Dihydroxy-3-(3,3-dichloroallyl)quinoline, the corresponding 4-mono and 2,4-dichloro derivatives, and substituted -(3-quinolyl)propionic acids were synthesized. -(2-Hydroxy-4-chloro-3-quinolyl) propiolactone was obtained from the latter.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 975–977, July, 1972.     

Synthesis,NMR and properties of a novel crown ether dimer: X-ray molecular structure of bis(2, 5-dimethoxy-4,6-dimethyl-1,3-xylyl)-18-crown-4

The synthesis and complete characterization of the precursor diol 3 and that of the crown ether 4 are reported. Further the X-ray structure of this novel crown ether is included, which provide us with valuable information about its solid-state structure. The title molecule lies about a centre of symmetry. Thus the novel 18-membered macrocycle 4 has a symmetrical configuration. Interestingly, a side view of the molecule shows that the two methoxy groups on each ring are on the same side, face to face and bend over the two arene units in the macrocycle. Finally, preliminary studies of its complexing property towards rhodium cations are presented and discussed. To cite this article: H. Amouri et al., C. R. Chimie 6 (2003).     

New derivatization method for determination of 3-chloro-4(dichloromethyl)-5-hydroxy-2(5H)-furanone in water

An extremely potent mutagen, 3-chloro-4(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX) is commonly present in chlorinated drinking water. Due to its high mutagenic activity and according to World Health Organization guidelines its concentration should be controlled in drinking waters. Determination of MX is difficult due to ppt levels at which the compound usually exists in drinking waters. Derivatization of MX with 2-propanol is presented as a method which significantly lowers the GC–MS detection level compared to other alcohol derivatization agents.     

二-(2-羟基-5-长链烷基苯基)-甲烷的合成

以脂肪酸、苯酚为原料, 经酰化反应、酯化反应、Fries重排、黄鸣龙还原等步骤, 得到正构长链烷基酚, 再与多聚甲醛在酸性催化剂下进行缩合反应, 生成二-(2-羟基-5-长链烷基苯基)-甲烷, 用核磁共振氢谱和碳谱、红外光谱和元素分析对产物进行了结构鉴定. 据上述反应路线, 以工业品壬基酚和多聚甲醛为原料, 合成出了二-(2-羟基-5-壬基苯基)-甲烷, 并对其工艺条件进行了研究. 结果表明, 选用草酸作催化剂, 烷基酚和甲醛物质的量比为2∶1, 130 ℃反应4 h, 产物产率达到60%, 且反应转化率和选择性分别为63%和95%.     

Synthesis of n-(2-chloro-5-bromo-4-pyrimidyl)- and N-(2-chloro-5-iodo-4-pyrimidyl)amino acids

The previously unreported N-(2-chloro-5-bromo-4-pyrimidyl)- and N-(2-chloro-5-iodo-4-pyrimidyl) amino acids were synthesized.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 527–529, April, 1971.     

Bis（4-chloro-2-cyclohexylimino methylphenolate）-two Thiocyanation Cadmium

1 INTRODUCTION Schiff base compounds have been of great interest for many years. These compounds are important systems in asymmetric catalysis and their transition metal complexes can often mimic biological sites, so they are of great significance as enzyme models. Their five- and six-coordinate complexes can disp- lay a variety of structural and magnetic properties. Complexes of d10 metal ion, such as cadmium (II), have aroused great attention since they are involved in many biological …     

Synthesis of 5-Alkyl(aryl)-2-alkylsulfanyl(alkoxy)-4-hydroxy-6H-1,3-oxazin-6-ones

Alkyl carbamates and S-alkyl thiocarbamates react with substituted malonyl dichlorides in boiling benzene to give the corresponding 2,5-substituted 4-hydroxy-6H-1,3-oxazin-6-ones. The reaction of S-methyl thiocarbamate with unsubstituted malonyl dichloride in boiling diethyl ether or benzene leads to formation of S-methyl (3-methylsulfanylaminocarbonyl-3-oxopropionyl)thiocarbamate and is not accompanied by cyclization, whereas in boiling toluene 4-hydroxy-2-methylsulfanyl-6H-1,3-oxazin-6-one is obtained.__________Translated from Zhurnal Obshchei Khimii, Vol. 75, No. 3, 2005, pp. 468–472.Original Russian Text Copyright © 2005 by Lalaev, Yakovlev, Zakhs.     

Oxidation of 4-methyl-4-(2-hydroxyethyl)-1,3-dioxane to 2-hydroxy-2-methylglutaric acid

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, p. 1284, September, 1988.     

Synthesis and modification of 4-hydroxy-2-methyl-3-(2-chloro-2-propenyl)quinoline

4-Hydroxy-2-methyl-3-(2-chloro-2-propenyl)quinoline was prepared by O-allylation of 4-hydroxy-2-methylquinoline followed by the Claisen rearrangement of the 2-methyl-4-(2-chloro-2-propenyloxy)quinoline obtained. Chemical modifications of 4-hydroxy-2-methyl-3-(2-chloro-2-propenyl)quinoline resulted in the synthesis of 4-amino-2-methyl-3-(2-methyl-3-indolyl)quinoline.