Category: 7686-78-4

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 7686-78-4, name is Diethyl 2-vinylcyclopropane-1,1-dicarboxylate, This compound has unique chemical properties. The synthetic route is as follows., Formula: C11H16O4

Preparation method: In air atmosphere,Add 0.2 mmol of N-pyrimidindolline compound to the microwave reaction tube,0.2 mmol of ethylene cyclopropane compound,0.006mmol of [Ru (p-cymene) Cl2] 2,0.06 mmol of mesitylene,0.04mmol of silver hexafluoroantimonate, microwave reaction at 40 C for 2 hours;After completion of the reaction, rinse with ethyl acetate.Chromatographic separation after concentration under reduced pressure (silica gel 200-300 mesh, eluent: ethyl acetate / petroleum ether gradient elution, ratio from 0/100 to 100/0)Dried to a pale yellow oil,Yield 75%, E / Z = 11: 1.

According to the analysis of related databases, 7686-78-4, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Zhengzhou University; Henan Communication Polytechnic College; Zhu Xinju; Wang Qiuling; Xie Xiaona; Zhang Xiaojie; Yan Jing; Xu Yan; Hao Xinqi; Song Maoping; (15 pag.)CN110551106; (2019); A;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Reference of 7686-78-4,Some common heterocyclic compound, 7686-78-4, name is Diethyl 2-vinylcyclopropane-1,1-dicarboxylate, molecular formula is C11H16O4, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

The preparation method is:In an air atmosphere,Add 0.2 mmol of N-pyrimidindolline compound to the microwave reaction tube,0.4mmol of ethylene cyclopropane compound,0.003mmol of [Ru (p-cymene) Cl2] 2,0.04mmol are trimethylbenzoic acid,0.02mmol of silver hexafluoroantimonate, microwave reaction at 25 C for 2 hours;After completion of the reaction, rinse with ethyl acetate.Chromatographic separation after concentration under reduced pressure (silica gel 200-300 mesh, eluent: ethyl acetate / petroleum ether gradient elution, ratio from 0/100 to 100/0),Dried to a pale yellow oil,Yield: 70%, E / Z = 20: 1.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route Diethyl 2-vinylcyclopropane-1,1-dicarboxylate, its application will become more common.

Reference:
Patent; Zhengzhou University; Henan Communication Polytechnic College; Zhu Xinju; Wang Qiuling; Xie Xiaona; Zhang Xiaojie; Yan Jing; Xu Yan; Hao Xinqi; Song Maoping; (15 pag.)CN110551106; (2019); A;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Adding a certain compound to certain chemical reactions, such as: 7686-78-4, name is Diethyl 2-vinylcyclopropane-1,1-dicarboxylate, belongs to esters-buliding-blocks compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 7686-78-4, Product Details of 7686-78-4

Preparation method: In air atmosphere,Add 0.2 mmol of N-pyrimidindolline compound to the microwave reaction tube,0.24 mmol of ethylene cyclopropane compound,0.003 mmol of [Ru (p-cymene) Cl2] 2, 0.06 mmol of 1-adamantanic acid,0.04 mmol of silver hexafluoroantimonate,Microwave at 50 C for 2 hours;After completion of the reaction, rinse with ethyl acetate.Chromatographic separation after concentration under reduced pressure (silica gel 200-300 mesh, eluent: ethyl acetate / petroleum ether gradient elution, ratio from 0/100 to 100/0)Dried to a pale yellow oil,The yield was 76% and E / Z> 20: 1.

At the same time, in my other blogs, there are other synthetic methods of this type of compound, Diethyl 2-vinylcyclopropane-1,1-dicarboxylate, and friends who are interested can also refer to it.

Reference:
Patent; Zhengzhou University; Henan Communication Polytechnic College; Zhu Xinju; Wang Qiuling; Xie Xiaona; Zhang Xiaojie; Yan Jing; Xu Yan; Hao Xinqi; Song Maoping; (15 pag.)CN110551106; (2019); A;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Synthetic Route of 7686-78-4, The chemical industry reduces the impact on the environment during synthesis 7686-78-4, name is Diethyl 2-vinylcyclopropane-1,1-dicarboxylate, I believe this compound will play a more active role in future production and life.

Preparation method: under an argon atmosphere, add 0.2 mmol of N-pyrimidine porphyrin compound, 0.36 mmol of ethylene cyclopropane compound to a 35 mL Shrek tube.0.008 mmol of [Cp*Rh(CH3CN)3](SbF6)2, 0.08 mmol of 1-adamantanic acid, 0.04 mmol of silver hexafluoroantimonate, methanol 0.5 mL, reacted at 90 C for 12 hours; after the reaction, using acetic acid Ethyl ester was rinsed, concentrated under reduced pressure, and then chromatographed on silica gel (200-300 mesh, eluent: ethyl acetate / petroleum ether gradient elution, ratio: 0/100 to 100/0). The yield was 81% and E/Z > 20:1.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, Diethyl 2-vinylcyclopropane-1,1-dicarboxylate, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Zhengzhou University; Zhu Xinju; Wang Qiuling; Zhi Changlei; Li Jing; Liu Shuang; Zhao Xuemei; Hao Xinqi; Song Maoping; (15 pag.)CN109180648; (2019); A;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Reference of 7686-78-4,Some common heterocyclic compound, 7686-78-4, name is Diethyl 2-vinylcyclopropane-1,1-dicarboxylate, molecular formula is C11H16O4, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

Preparation method: In air atmosphere,Add 0.2 mmol of N-pyrimidindolline compound to the microwave reaction tube,0.36 mmol of ethylene cyclopropane compound,0.008mmol of [Ru (p-cymene) Cl2] 2,0.08 mmol mesitylene,0.04mmol of silver hexafluoroantimonate, microwave reaction at 60 C for 1 hour;After completion of the reaction, rinse with ethyl acetate.Chromatographic separation after concentration under reduced pressure (silica gel 200-300 mesh, eluent: ethyl acetate / petroleum ether gradient elution, ratio from 0/100 to 100/0)Dried to a pale yellow oil,Yield: 81%, E / Z> 20: 1.

The synthetic route of 7686-78-4 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Zhengzhou University; Henan Communication Polytechnic College; Zhu Xinju; Wang Qiuling; Xie Xiaona; Zhang Xiaojie; Yan Jing; Xu Yan; Hao Xinqi; Song Maoping; (15 pag.)CN110551106; (2019); A;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics