1 Introduction Anhydrous sodium,mainly produced in the United States,Canada,Japan,is indispensable commodities and raw materials in daily life and industry.In recent years,anhydrous sodium sulfate of general size was ...1 Introduction Anhydrous sodium,mainly produced in the United States,Canada,Japan,is indispensable commodities and raw materials in daily life and industry.In recent years,anhydrous sodium sulfate of general size was much oversupplied[1].However particles anhydrous sodium sulphate of large size is not adequate to the demand for its展开更多
Summary:Sodium bisulfite could add to the central methine bridge of biliver- din in methanol,and give sodium bilirubin-10-sulfonate,however no bilirubin was formed.
N,N-deithyl-iododifluoroacetamide 1 reacted with alkenes,alkynes in aqueous aceto- nitrile solutions of sodium dithionite and sodium hydrogen carbonate at room temperature to give the corresponding adducts,thus consti...N,N-deithyl-iododifluoroacetamide 1 reacted with alkenes,alkynes in aqueous aceto- nitrile solutions of sodium dithionite and sodium hydrogen carbonate at room temperature to give the corresponding adducts,thus constituting a new method for introducing the CF_2 group into organic mol- ecules.Compound 1 reacted with conjugated olefins 2b,c to afford the iodine-free adducts 7b,c. The adducts 3d-f,from addition of 1 to alkenes 2d-f,could be converted into α,α-difluoro-γ- lactones 5d-f by treatment with silica gel.Compound 1 reacted with ethyl vinyl ether 2i to give aldehyde 8,and perfluoroalkyl or polyfluoroalkyl iodides reacted similarly.A radical mechanism was proposed for the addition reaction.Under the same condition,N,N-diethyl-bromodifluoroacetamide produced only the corresponding sulfinate Et_2NC(O)CF_2SO_2Na.展开更多
Reaction of perfluoroalkyl iodides with a series of alkynes under sulfinatodehalogenation condition gave a mixture of E/Z adducts very readily in high yield, thus constituted a mild, convenient and effective new metho...Reaction of perfluoroalkyl iodides with a series of alkynes under sulfinatodehalogenation condition gave a mixture of E/Z adducts very readily in high yield, thus constituted a mild, convenient and effective new method for the addition of perfluoroalkyl iodides to alkynes. Under the same con- dition, in the presence of 1-hexyne perfluoroalkyl bromide and 1,1,1-trichlorotrifluoroethane reacted only to give sulfinates as the major products. A radical mechanism was proposed for the addition reaction.展开更多
The addition of sodium perfluoroalkanesulfinates (R_FSO_2Na) to various olefins (CH_2=CHR) initiated by Fenton reagent (Fe^(2+)-H_2O_2) in the presence of sodium azide gave the adduets R_FCH_2- CHN_3R in good yield.A ...The addition of sodium perfluoroalkanesulfinates (R_FSO_2Na) to various olefins (CH_2=CHR) initiated by Fenton reagent (Fe^(2+)-H_2O_2) in the presence of sodium azide gave the adduets R_FCH_2- CHN_3R in good yield.A radical mechanism was proposed based on the EPR and other evidences. The adducts were readily reduced through catalytic hydrogenation to give the corresponding amines R_FCH_2CH(NH_2)R in high yield.The reaction represents a convenient and effective route to these useful organofluorine compounds.展开更多
Polyfluoroalkyl iodides reacted with olefins in aqueous DMF solution of sodium disulfite under mild conditions to give the corresponding 1:1 adducts in good yields,providing a convenient polyfluoroalkylation method.Th...Polyfluoroalkyl iodides reacted with olefins in aqueous DMF solution of sodium disulfite under mild conditions to give the corresponding 1:1 adducts in good yields,providing a convenient polyfluoroalkylation method.This indicated that R_F radicals were formed in the reaction of polyfluoroalkyl iodides and sodium disulfite.A SET mechanism is proposed for the sulfinatodehalogenation reaction of sodium disulfite.展开更多
基金financial support of National Nature Science Foundation (21376178)TIDA giant growth plan (2011-XJR13020)+3 种基金Tianjin Science and technology support program (12ZCDZSF06900)Tianjin University of Science and Technology fund for scientific research (20120119)Tianjin education commission program (20130509)Research fund for the doctoral program of higher education of China (20131208120001)
文摘1 Introduction Anhydrous sodium,mainly produced in the United States,Canada,Japan,is indispensable commodities and raw materials in daily life and industry.In recent years,anhydrous sodium sulfate of general size was much oversupplied[1].However particles anhydrous sodium sulphate of large size is not adequate to the demand for its
基金This work was supported by the Natural Science Funda-tion of China(86020219)
文摘Summary:Sodium bisulfite could add to the central methine bridge of biliver- din in methanol,and give sodium bilirubin-10-sulfonate,however no bilirubin was formed.
文摘N,N-deithyl-iododifluoroacetamide 1 reacted with alkenes,alkynes in aqueous aceto- nitrile solutions of sodium dithionite and sodium hydrogen carbonate at room temperature to give the corresponding adducts,thus constituting a new method for introducing the CF_2 group into organic mol- ecules.Compound 1 reacted with conjugated olefins 2b,c to afford the iodine-free adducts 7b,c. The adducts 3d-f,from addition of 1 to alkenes 2d-f,could be converted into α,α-difluoro-γ- lactones 5d-f by treatment with silica gel.Compound 1 reacted with ethyl vinyl ether 2i to give aldehyde 8,and perfluoroalkyl or polyfluoroalkyl iodides reacted similarly.A radical mechanism was proposed for the addition reaction.Under the same condition,N,N-diethyl-bromodifluoroacetamide produced only the corresponding sulfinate Et_2NC(O)CF_2SO_2Na.
文摘Reaction of perfluoroalkyl iodides with a series of alkynes under sulfinatodehalogenation condition gave a mixture of E/Z adducts very readily in high yield, thus constituted a mild, convenient and effective new method for the addition of perfluoroalkyl iodides to alkynes. Under the same con- dition, in the presence of 1-hexyne perfluoroalkyl bromide and 1,1,1-trichlorotrifluoroethane reacted only to give sulfinates as the major products. A radical mechanism was proposed for the addition reaction.
基金the National Natural Science Foundation of China
文摘The addition of sodium perfluoroalkanesulfinates (R_FSO_2Na) to various olefins (CH_2=CHR) initiated by Fenton reagent (Fe^(2+)-H_2O_2) in the presence of sodium azide gave the adduets R_FCH_2- CHN_3R in good yield.A radical mechanism was proposed based on the EPR and other evidences. The adducts were readily reduced through catalytic hydrogenation to give the corresponding amines R_FCH_2CH(NH_2)R in high yield.The reaction represents a convenient and effective route to these useful organofluorine compounds.
文摘Polyfluoroalkyl iodides reacted with olefins in aqueous DMF solution of sodium disulfite under mild conditions to give the corresponding 1:1 adducts in good yields,providing a convenient polyfluoroalkylation method.This indicated that R_F radicals were formed in the reaction of polyfluoroalkyl iodides and sodium disulfite.A SET mechanism is proposed for the sulfinatodehalogenation reaction of sodium disulfite.
