Patents Assigned to Nutrichem Company Limited
-
Patent number: 10253001Abstract: The present invention discloses a method for preparing azoxystrobin intermediates represented by formulae (1) and (2), comprising: controlling a compound represented by formula (3) to contact with sodium methoxide and 4,6-dichloropyrimidine, to obtain a mixture of intermediates represented by formulae (1) and (2), in the existence of a catalyst, the catalyst is an azabicyclic compound or its salt. The present invention further discloses a method for preparing azoxystrobin, comprising: controlling the intermediate represented by formula (2) provided in the present invention to react with 2-cyanophenol or its salt under the catalytic action of an azabicyclic compound or its salt, to obtain an azoxystrobin compound represented by formula (4). The method provided in the present invention has advantages including high transformation ratio, high product purity, easy and convenient operation, and environmental friendliness.Type: GrantFiled: January 19, 2018Date of Patent: April 9, 2019Assignees: Nutrichem Company Limited, Shangyu Nutrichem Co., LTD.Inventors: Jianwei Chen, Wenjun Wang, Jianhong Chi, Yongchang Zhao, Xufang Deng, Long Wang, Wentao Jin, Guobin Chen
-
Publication number: 20180141918Abstract: The present invention discloses a method for preparing azoxystrobin intermediates represented by formulae (1) and (2), comprising: controlling a compound represented by formula (3) to contact with sodium methoxide and 4,6-dichloropyrimidine, to obtain a mixture of intermediates represented by formulae (1) and (2), in the existence of a catalyst, the catalyst is an azabicyclic compound or its salt. The present invention further discloses a method for preparing azoxystrobin, comprising: controlling the intermediate represented by formula (2) provided in the present invention to react with 2-cyanophenol or its salt under the catalytic action of an azabicyclic compound or its salt, to obtain an azoxystrobin compound represented by formula (4). The method provided in the present invention has advantages including high transformation ratio, high product purity, easy and convenient operation, and environmental friendliness.Type: ApplicationFiled: January 19, 2018Publication date: May 24, 2018Applicants: Nutrichem Company Limited, Shangyu Nutrichem CO., LTD.Inventors: Jianwei Chen, Wenjun Wang, Jianhong Chi, Yongchang Zhao, Xufang Deng, Long Wang, Wentao Jin, Guobin Chen
-
Patent number: 9920015Abstract: The present invention discloses a method for preparing azoxystrobin intermediates represented by formulae (1) and (2), comprising: controlling a compound represented by formula (3) to contact with sodium methoxide and 4,6-dichloropyrimidine, to obtain a mixture of intermediates represented by formulae (1) and (2), in the existence of a catalyst, the catalyst is an azabicyclic compound or its salt. The present invention further discloses a method for preparing azoxystrobin, comprising: controlling the intermediate represented by formula (2) provided in the present invention to react with 2-cyanophenol or its salt under the catalytic action of an azabicyclic compound or its salt, to obtain an azoxystrobin compound represented by formula (4). The method provided in the present invention has advantages including high transformation ratio, high product purity, easy and convenient operation, and environmental friendliness.Type: GrantFiled: March 11, 2014Date of Patent: March 20, 2018Assignees: NUTRICHEM COMPANY LIMITED, SHANGYU NUTRICHEM CO., LTD.Inventors: Jianwei Chen, Wenjun Wang, Jianhong Chi, Yongchang Zhao, Xufang Deng, Long Wang, Wentao Jin, Guobin Chen
-
Patent number: 9611226Abstract: Disclosed in the present invention is a preparation method of azoxystrobin having a structure as shown by formula (1), the method comprising: a) performing an etherification reaction by reacting the compound having a structure shown by formula (2) with 2-cyanophenol and/or a salt thereof under the catalysis of an azabicyclo tertiary amine compound and/or a salt thereof as the catalyst in a butyl acetate medium to obtain a butyl acetate solution containing azoxystrobin; and b) cooling the butyl acetate solution containing azoxystrobin to precipitate Azoxystrobin having a structure as shown by formula (1) from the butyl acetate solution. Using the method provided by the present invention to prepare azoxystrobin can significantly improve the yield of azoxystrobin, and can obtain azoxystrobin products having high purity.Type: GrantFiled: March 20, 2014Date of Patent: April 4, 2017Assignees: Nutrichem Company Limited, Shanqyu Nutrichem Co., Ltd.Inventors: Wenjun Wang, Jianwei Chen, Jianhong Chi, Yongchang Zhao, Xufang Deng, Long Wang, Hua'nan You
-
Patent number: 9556128Abstract: The present invention relates to a method for preparing an acrylate compound. The acrylate compound has a structure as shown in formula (I). The method includes: subjecting a compound with a structure of formula (II) or a mixture of compounds with structures of formula (I) and formula (II), and a catalyst to a contact reaction in the absence of an anhydride, and removing the resulting methanol by pressure reduced distillation during the contact reaction process. In the formulas (I) and (II), R is selected from one of: an alkoxy with a carbon number of 1-5, a substituent-containing phenoxyl with a carbon number of 6-20, a substituent-containing heteroaryloxy with a carbon number of 4-20, a substituent-containing heteroaryloxymethyl with a carbon number of 4-20, a substituent-containing phenoxymethyl with a carbon number of 5-20, and a substituent-containing alkyl with a carbon number of 2-20.Type: GrantFiled: March 20, 2014Date of Patent: January 31, 2017Assignees: NUTRICHEM COMPANY LIMITED, SHANGYU NUTRICHEM CO., LTD.Inventors: Xufang Deng, Wenjun Wang, Jianwei Chen, Yongchang Zhao, Jianhong Chi, Long Wang, Hua'nan You
-
Patent number: 8278445Abstract: Preparation method of a compound of general formula (I) comprises the following steps: (1) a compound of general formula (II) reacts with a formylating agent in an aprotic solvent at a temperature between ?20° C. and 200° C. in the presence of a Lewis acid, then an organic base is added to promote the reaction to obtain an intermediate product; (2) the above intermediate product reacts with a methylating agent in the presence of an alkali at a temperature between ?20° C. and 100° C. to obtain the compound of formula (I).Type: GrantFiled: September 19, 2008Date of Patent: October 2, 2012Assignee: Nutrichem Company LimitedInventors: Shangzhong Liu, Canxian Mu, Wenjun Wang, Jianwei Chen, Shuguang Wang