855423-12-0Relevant academic research and scientific papers
Reusable cobalt-phthalocyanine in water: Efficient catalytic aerobic oxidative coupling of thiols to construct S-N/S-S bonds
Dou, Yingchao,Huang, Xin,Wang, Hao,Yang, Liting,Li, Heng,Yuan, Bingxin,Yang, Guanyu
supporting information, p. 2491 - 2495 (2017/07/17)
A new aerobic oxidative coupling of thiols in water to construct sulfenamides or disulfides was developed, utilizing cobalt(ii)phthalocyanine-tetra-sodium sulfonate as the catalyst and O2 as the oxidant. The mother liquor could be recycled up to 20 times with negligible loss of activity and only a minor decrease of product yield.
Method for catalyzing molecular oxygen to oxidize into disulfides with S-S bonds in aqueous phase
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Paragraph 0022; 0023; 0029; 0030, (2017/08/29)
The invention provides a method for catalyzing molecular oxygen to oxidize into disulfides with S-S bonds in an aqueous phase. The method includes taking water-soluble transition metal phthalocyanine compounds as catalysts, and enabling sulfhydryl compounds to react for 1-30 hours in the aqueous phase at a pressure of 0.01-1.00 Mpa, at 40-100 DEG C and in the presence of oxygen or air so as to obtain the disulfides with the S-S bonds. The method has the advantages that reaction is conducted in the aqueous phase, so that addition of other organic solvents is unneeded; the catalysts are high in catalytic activity, high in reaction efficiency and reusable; the method is simple in synthetic process, high in product selectivity, fewer in byproducts and wastes and environment friendly, thereby being promising in industrial application prospect.
Unsymmetrical disulfide and sulfenamide synthesis via reactions of thiosulfonates with thiols or amines
Taniguchi, Nobukazu
, p. 2030 - 2035 (2017/03/17)
The reactivity of thiosulfonates with nucleophilic reagents was investigated. When reactions of thiosulfonates with thiols were performed, unsymmetrical disulfides were obtained in excellent yields. This procedure could employ numerous aryl or alkyl thiols. On the other hand, reactions of thiosulfonates with amines proceeded in the presence of a copper catalyst. The procedure was performed efficiently in air, and afforded the corresponding sulfenamides.
A versatile and convenient preparation of unsymmetrical diaryl disulfides
Demkowicz, Sebastian,Rachon, Janusz,Witt, Dariusz
body text, p. 2033 - 2038 (2009/04/03)
We have developed a convenient method for the synthesis of unsymmetrical diaryl disulfides under mild conditions in excellent yields. The described method is based on the straightforward preparation of 5,5-dimethyl-2-thioxo-1,3, 2-dioxaphosphorinane-2-sulfenyl bromide from readily available 5,5-dimethyl-2-sulfanyl-2-thioxo-l,3,2-dioxaphosphorinane or bis(5,5-dimethyl-2-thioxo-l,3,2-dioxaphosphorinan-2-yl) disulfide. The unsymmetrical diaryl disulfides can be obtained from aromatic thiol derivatives bearing electron-withdrawing or electron-donating groups. Thieme Stuttgart.
