50583-51-2Relevant articles and documents
Preparation method of di-p-methoxybenzoyl tartaric acid
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Paragraph 0015; 0019-0025, (2020/04/22)
The invention relates to a preparation method of di-p-methoxybenzoyl tartaric acid. The method comprises the following steps: 1) adding tartaric acid and methoxybenzoyl chloride into a reaction bottleat room temperature, adding a reaction solvent, a chlorination reagent and a catalyst to react, heating for reflux after anhydride is generated after the reaction is completed, cooling to 50-55 DEG C, adding a hydrolysis solvent and water, heating to 80-85 DEG C, and reacting for 0.5-3.5 hours; adding a crystallization solvent, cooling to 65-70 DEG C, adding a seed crystal, slowly cooling to 40-55 DEG C, carrying out a crystallization reaction, cooling, carrying out suction filtration, leaching, and drying to obtain the product. The method provided by the invention has the advantages of simple process flow, less equipment investment, one-pot operation, low labor intensity, product purity of 99% or more, and molar yield of 95% or more.
Novel processes for the preparation of (R)-alpha-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4-piperidinemethanol
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, (2008/06/13)
The present invention provides various processes for the preparation of (R)-α-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4-piperidinemethanol. These processes may be characterized by the following scheme:
Novel processes for the preparation or (R)-alpha-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4-piperidinemethanol
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, (2008/06/13)
The present invention provides various processes for the preparation of (R)-α-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4-piperidinemethanol. These processes may be characterized by the following scheme: