1,1,1,-Trifluoro-2- substituted- phenyl- 2- propanols- 3- 14C were prepared from addition of methyl- 14C magnesium iodide to appropriate trifluoroacetophenone. These alcohols were converted into tosylatcs by reaction ...1,1,1,-Trifluoro-2- substituted- phenyl- 2- propanols- 3- 14C were prepared from addition of methyl- 14C magnesium iodide to appropriate trifluoroacetophenone. These alcohols were converted into tosylatcs by reaction with n-butyllithium and then with p-toluenesulfonyl chloride. The yield, boiling point or melting point and pertinent spectral data of these compounds are reported.展开更多
An efficient synthesis of benzoxazole-substituted 3,4-dihydropyrimidinones （DHPMs） using trifluoro acetic acid as the catalyst for the first time from an aldehyde, 13-keto ester and benzoxazole-substituted urea/thio...An efficient synthesis of benzoxazole-substituted 3,4-dihydropyrimidinones （DHPMs） using trifluoro acetic acid as the catalyst for the first time from an aldehyde, 13-keto ester and benzoxazole-substituted urea/thiourea under solvent-free conditions is described. Compared to the classical Biginelli reaction conditions, this new method consistently has the advantage of excellent yields （80-91%） and short reaction time （40-130 min） at reflux temperature. 2009 M. Adharvana Chad. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.展开更多
Reaction of diethyl 2,2-difluoro-3-（a-methylbenzyl）imino-4,4,4-trifluoropropanephosphonate （3） with triethylamine afforded a mixture of normal [1,3]-proton shift reaction product 5 and its HF-eliminated compound 6...Reaction of diethyl 2,2-difluoro-3-（a-methylbenzyl）imino-4,4,4-trifluoropropanephosphonate （3） with triethylamine afforded a mixture of normal [1,3]-proton shift reaction product 5 and its HF-eliminated compound 6Z in 1 ： 1 ratio. Upon hydrolysis, this reaction mixture gave solely 1,3,3,3-tetrafluoro-2-dioxypropanephosphonate （9）. Reaction of 3 with DBU provided only 6, in which the ratio of E/Z forms was dependent on the reaction conditions. Aqueous hydrolysis of 6 led to 9. Catalytic hydrogenation and hydrogenolysis of 6 gave geometric isomers of 11 as expected. The reaction mechanism involved was discussed.展开更多
Title Compond-5 chloro 2,4,6 trifluoro 1,3 bezenedicarbonitrile was prepared by fluoration exchange reaction under comparatively mild condition with yield 81%;various reactive conditions,as well as its possible by pro...Title Compond-5 chloro 2,4,6 trifluoro 1,3 bezenedicarbonitrile was prepared by fluoration exchange reaction under comparatively mild condition with yield 81%;various reactive conditions,as well as its possible by products,were discussed in detail.The structure of the target compound was confirmed by excluding its two isomers based on IR,MS, 13 CNMR,and 19 FNMR data.展开更多
基金The Project Supported by the National Science Foundation of U.S.A.
文摘1,1,1,-Trifluoro-2- substituted- phenyl- 2- propanols- 3- 14C were prepared from addition of methyl- 14C magnesium iodide to appropriate trifluoroacetophenone. These alcohols were converted into tosylatcs by reaction with n-butyllithium and then with p-toluenesulfonyl chloride. The yield, boiling point or melting point and pertinent spectral data of these compounds are reported.
文摘An efficient synthesis of benzoxazole-substituted 3,4-dihydropyrimidinones （DHPMs） using trifluoro acetic acid as the catalyst for the first time from an aldehyde, 13-keto ester and benzoxazole-substituted urea/thiourea under solvent-free conditions is described. Compared to the classical Biginelli reaction conditions, this new method consistently has the advantage of excellent yields （80-91%） and short reaction time （40-130 min） at reflux temperature. 2009 M. Adharvana Chad. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
基金Project supported by the National Natural Science Foundation of China （Nos. 20272075. 20372076）. Dedicated to Professor Xikui Jiang on the occasion of his 80th birthday.
文摘Reaction of diethyl 2,2-difluoro-3-（a-methylbenzyl）imino-4,4,4-trifluoropropanephosphonate （3） with triethylamine afforded a mixture of normal [1,3]-proton shift reaction product 5 and its HF-eliminated compound 6Z in 1 ： 1 ratio. Upon hydrolysis, this reaction mixture gave solely 1,3,3,3-tetrafluoro-2-dioxypropanephosphonate （9）. Reaction of 3 with DBU provided only 6, in which the ratio of E/Z forms was dependent on the reaction conditions. Aqueous hydrolysis of 6 led to 9. Catalytic hydrogenation and hydrogenolysis of 6 gave geometric isomers of 11 as expected. The reaction mechanism involved was discussed.
文摘Title Compond-5 chloro 2,4,6 trifluoro 1,3 bezenedicarbonitrile was prepared by fluoration exchange reaction under comparatively mild condition with yield 81%;various reactive conditions,as well as its possible by products,were discussed in detail.The structure of the target compound was confirmed by excluding its two isomers based on IR,MS, 13 CNMR,and 19 FNMR data.
