New downstream synthetic route of 2-((4-Methoxyphenyl)ethynyl)aniline

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 157869-15-3, name is 2-((4-Methoxyphenyl)ethynyl)aniline, A new synthetic method of this compound is introduced below., COA of Formula: C15H13NO

General procedure: To a microwave vial, a mixture of 2-alkynylaniline (1 equiv), sulfonyl hydrazide (1.5 equiv), I2 (10 mol%) and pTSA (50 mol%) was taken in 1,4-dioxane irradiated for 15 min at 110C, 100W in CEM microwave synthesizer. The progress and completion of reaction is monitored by TLC using EtOAc/n-Hexane (1:10) as an eluent. The reaction mixture was then cooled to room temperature and extracted with ethyl acetate. The combined organic phase was washed with sodium thiosulphate (50 mL) and dried over Na2SO4. After filtration and evaporation of the solvents in vacuum, the mixture of products was separated by column chromatography on silica gel (EtOAc/n-hexane: 1:10) to yield the desired product 3.

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference:
Article; Sharma, Shivani; Pathare, Ramdas S.; Sukanya; Maurya, Antim K.; Goswami, Bhagyashree; Agnihotri, Vijai K.; Sawant, Devesh M.; Pardasani, Ram T.; Tetrahedron Letters; vol. 58; 40; (2017); p. 3823 – 3826;,
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Brief introduction of 157869-15-3

The synthetic route of 157869-15-3 has been constantly updated, and we look forward to future research findings.

Electric Literature of 157869-15-3,Some common heterocyclic compound, 157869-15-3, name is 2-((4-Methoxyphenyl)ethynyl)aniline, molecular formula is C15H13NO, 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.

General procedure: A sealed tube was charged with the mixture of 2-alkynylaniline 1 (1 mmol), carbon disulfide (1.5 mmol), then stirred in a solution of DBUH+ in CH3CN (1.5 mL) at room temperature under nitrogen atmosphere for indicated time. After completion, then H2O (5 mL) was added and the mixture was extracted with EtOAc (5 mL x 3), dried by anhydrous Na2SO4. Evaporation of the solvent followed by purification on silica gel (petroleum ether/ethylacetate = 4/1) provided the corresponding product 2.

The synthetic route of 157869-15-3 has been constantly updated, and we look forward to future research findings.

Reference:
Article; Zhao, Peng; Liao, Qian; Gao, Hongxin; Xi, Chanjuan; Tetrahedron Letters; vol. 54; 19; (2013); p. 2357 – 2361;,
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Share a compound : 2-((4-Methoxyphenyl)ethynyl)aniline

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 2-((4-Methoxyphenyl)ethynyl)aniline, and friends who are interested can also refer to it.

As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 157869-15-3 name is 2-((4-Methoxyphenyl)ethynyl)aniline, This compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below. 157869-15-3

In 15 ml reaction tube are sequentially added into a 1 l (0.3 mmol, 67 mg), [RhCp * Cl2 ]2 (0.015 Mmol, 9.3 mg) and hexafluoroisopropanol (2 ml), in a nitrogen atmosphere of the reaction pipe sealing, in the 120 C stirring for 20 h. After the reaction, the reaction tube to be cooled to the room temperature, adding 10 ml water, then the extraction of ethyl acetate (10 ml ¡Á 3), after the organic phase with water and saturated salt water are successively washing, drying with anhydrous sodium sulfate. Filtering, turns on lathe does, too separating by silica gel column (petroleum ether/ethyl acetate=10/1) to yellow solid product 2 l (44 mg, 65%). The compound of the characterization data are as follows

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 2-((4-Methoxyphenyl)ethynyl)aniline, and friends who are interested can also refer to it.

Reference:
Patent; Henan Normal University; Fan Xuesen; Jia Ruixue; Zhang Xinying; Li Bin; (19 pag.)CN110105274; (2019); A;,
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem