Wet cyanuric chloride promoted efficient synthesis of amidoalkyl naphthols under solvent-free conditions

An efficient and direct procedure has been developed for the preparation of amidoalkyl naphthols by a one-pot condensation of aryl aldehydes, 2-naphthol and urea or amides, in the presence of wet-cyanuric chloride （wet-TCT） as a catalyst. The reactions were carried out under solvent-free media. The present methodology offers several advantages such as excellent yields, simple procedure and eco-friendly reaction condition.

A facile synthesis of novel optically active R,R-2-(4-(2-(4-(5-chloro-3-halo-pyridin-2-yloxy)-phenoxy)-propionyloxy)-phenoxy)-propionic acid esters using cyanuric chloride as potential herbicide

A facile method for the synthesis of a new series of R,R-2-（4-（2-（4-（5-chloro-3-halopyridin-2-yloxy）-phenoxy）-propionyloxy）-phenoxy） -propionic acid ester derivatives containing a halo-substituted pyridine carrying two R,R chiral centers from（R）-2-（4- hydroxyphenoxy）propionic acid,halopyridines and alcohols using base/cyanuric chloride/catalyst system is reported.Their herbicidal activities against grass weeds and crops selectivity were evaluated.

Cyanuric chloride-catalyzed synthesis of 10-aryl-6,8-dimethyl-6,10-dihydro-5-oxa-6,8-diazaanthra[2,3-d][1,3]dioxole-7,9-diones

An environmentally friendly procedure for the preparation of 10-aryl-6,8-dimethyl-6,10-dihydro-5-oxa-6,8-diazaanthra[2,3- d] [ 1,3]dioxole-7,9-diones under thermal solvent-free conditions in the presence of cyanurie chloride as heterogeneous catalyst was developed.

PREPARATION AND ADSORPTION OF THIOUREA MODIFIED GLUTARALDEHYDE-CROSSLINKED CHITOSAN RESINS

The preparation and adsorption of thiourea modified glutaraldehyde-crosslinked chitosan resin （Thio-chitosan） using cyanuric chloride as activator was studied. The adsorptive capacity of thio-chitosan with 15% apparent degree of crosslinking （DC, mass ration of glutaraldehyde to chitosan） to Cu（Ⅱ） was 160mg/g （dry weight）. The adsorption of Cu（Ⅱ） was correlated with Freundlich and Langmuir isotherm equation. Cu（Ⅱ） adsorbed on thio-chitosan column （ 1cm×10cm） was eluted with 0.5mol/L H2SO4, 6mol/L HCI and 3% thiourea solution with the recovery of 88.3%, 86.1% and 95.3%, respectively. The thio-chitosan resin can be applied to the separation and recovery of metal ions.

Facile Synthesis of Dendritic Hydroxyl-terminated Cyanuric Chloride Derivatives and Their Properties

Novel dendritic compounds G1.5（OH）4 and G1.5（OH）8 with peripheral hydroxyl were synthesized under mild conditions from eyanuric chloride, ethylene diamine, ethanolamine and diethanolamine. The products could be separated and purified through dispersion and precipitation in organic solvents with good yields （over 93.0%） and high purity （above 98.0%, HPLC）. The structures of the products were characterized by 1R, MS, 1H NMR and elementary analysis. G1.5（OH）4 and Gl.5（OH）8 could be dissolved in polar solvents such as methanol, water and dimethylsulfoxide. TGA analysis showed that G1.5（OH）4 and G1.5（OH）8 had good thermo stability. The aqueous solutions ofG1.5（OH）4 and G1.5（OH）8 exhibited low surface tension.

Antimicrobial M aterials: Synthesis of Reactive 5,5-Dimethylhydantoin Derivative and Application in Cellulose with Dyeing Process

The efficient and regenerable antibacterial properties of Nhalamines make them an ideal candidate for parapretion of antimicrobial textiles. In this study,a 5,5-dimethylhydantoin-based reactive N-halamine precursor, 4-( 4-( 3-( 3-hydroxypropyl)-5,5-dimethylhydantoin)-6-chloro-1,3,5-triazinylamino)-benzenesulfonate( HTB), was synthesized and characterized by ~1H-NMR. The synthesized compound was coated to cotton fabrics via reactive dye dyeing process. The coated cotton showed excellent antimicrobial activities against S. aureus( Gram-positive) and E. coli O157: H7( Gram-negative) with short contact times after exposing to diluted household bleach. The treatment method used in this study has a small effect on the tensile strength of cotton fabrics. The durability and regenerability of the chlorinated cotton samples were tested.Although the chlorine content decreased towards washing and storage,almost all of the initial oxidative chlorine levels could be regained after rechlorination.

Study on novel eco-friendly anti-creasing agents for natural silk fabric

Three novel eco-friendly anti-creasing agents have been designed and synthesized. The natural silk fabrics treated with them exhibit higher wrinkle recovery degree, strength retention rate and whiteness than those finished with 1,2,3,4-butane tetracarboxylic acid （BTCA）. The washing durability of the fabrics treated with the synthesized compounds and BTCA is similar. The chlorine atom, the carboxyl and the s-triazine ring in the synthesized structures and the surface roughness of the silk fabric are all contributive to the imorovement of the crease resistance of silk.

Targeted synthesis of novel porous aromatic frameworks with selective separation of CO_2/CH_4and CO_2/N_2

Novel porous aromatic frameworks（PAF-53 and PAF-54） have been obtained by the polymerization of amino compound（p-phenylenediamine and melamine） and cyanuric chloride. They display a certain amount of CO2 adsorption capacity and highly selective separation of CO2/CH4 and CO2/N2 as 18.1 and83 by Henry Law respectively. They may be applied as ideal adsorbents to separate and capture CO2.

A simple and expedient method for the stepwise synthesis of 2-ethoxy-(4H)-3,1-benzoxazine-4-ones

A simple and practical route is described for the synthesis of 2-efhoxy-（4H）-3,1 -benzoxazine-4-ones using the coupling reaction of anthranilic acid derivatives with diethyl dicarbonate following with fast cyclization of the carbamate adduct with a dehydrocyclization agent such as cyanuric chloride and N,N′-dicyclohexylcarbodiimide in PEG at room temperature.High yields of the products obtained under mild reaction conditions with simple work-up of the reaction mixture.

Synthesis and Biological Activities of Novel s-Triazine Bridged Dinucleoside Analogs

A series of novel dinucleosides linked by s-triazine were synthesized via the nucleophilic substitution reaction of amino nucleoside and cyanuric chloride in THF/H20. The biological activities of these novel dinucleoside analogs against HIV-RT, HeLa and A-549 cell lines in vitro were evaluated.