214285-87-7

Upstream product

• 104-94-9 4-methoxy-aniline 
• 78-95-5 chloroacetone 

Downstream Products

• 910042-25-0 N-(4-methoxyphenyl)-N-(2-oxopropyl)-(E)-3-phenylpropenamide 
• 94437-07-7 1,1-bis(4-(dimethylamino)phenyl)propan-2-one 
• 1374162-54-5 C₁₇H₁₉NO₂ 
• 1374162-53-4 (R)-2-(4-methoxyphenyl)-4-methyl-1,2,3,4-tetrahydroisoquinolin-4-ol 
• 1374162-40-9 1-[(4-methoxyphenyl)({[2-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl})amino]propan-2-one 
• 1115390-09-4 C₁₈H₁₉NO₄ 
• 1032606-37-3 ethyl (E)-3-[N-(4-methoxyphenyl)-N-(3-oxopropyl)carbamoyl]acrylate 
• 1032606-33-9 N-(4-methoxyphenyl)-N-(2-oxopropyl)-(E)-4-methylpent-2-enamide 
• 1032606-92-0 ethyl (E)-4-(4-methoxyphenyl-2-oxopropylamino)but-2-enoate 
• 1032606-31-7 N-(4-methoxyphenyl)-N-(2-oxopropyl)-(E)-but-2-enamide 
• 910042-24-9 N-(4-methoxyphenyl)-N-(2-oxopropyl)propenamide 
• 910042-26-1 N-(4-methoxyphenyl)-N-(2-oxopropyl)-(E)-3-(2-methoxyphenyl)propenamide 

Relevant academic research and scientific papers

Amine alkylation reaction continuous flow process

The invention relates to an amine alkylation reaction continuous flow process, in particular to a method for preparing an alkoxy amine acetone compound through the amine alkylation reaction continuousflow process. A raw material alkoxy aniline organic sol

Preparation method of 4-AA key intermediate epoxy butylamide

The invention relates to a preparation method of 4-AA key intermediate epoxy butylamide. The preparation method comprises the steps that (1) synthesis of epoxy butyric acid is conducted: a starting material L-threonine is cyclized under diazotization and

Preparation method of N-acetonyl amine compound

The invention discloses a preparation method of an N-acetonyl amine compound. The method comprises the following steps that an amine compound and glycerin are used as reaction raw materials, and in the presence of a composite catalyst and an alkali addition agent, in reaction mediums and at the reaction temperature of 80-180 DEG C, a reaction is performed for 2-48 hours in a sealed reactor so that the N-acetonyl amine compound is obtained. The method disclosed by the invention is simple, reaction conditions are mild, target products can be obtained at a low cost and at a high yield, and the used catalyst has high catalytic activity and is easy to separate and repeatedly use in a reaction system; besides, the whole process is environment-friendly, and the utilization of by-products namely the glycerin of biologic diesel oil is promoted.

Diastereoselective cobalt-catalyzed reductive aldol cyclizations using diethylzinc as the stoichiometric reductant

Cobalt catalysis enables a new method for the generation of zinc enolates using diethylzinc to reduce α,β-unsaturated amides. This method has been applied to a high-yielding diastereoselective reductive aldol cyclization.