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4-dimethylaminopyridine, commonly referred to as DMAP, is a strong nucleophilic acylation catalyst. The resonance of the electron-donating dimethylamino group with the parent ring (pyridine ring) can strongly activate the nitrogen atoms on the ring for nucleophilic substitution, and significantly catalyze the acylation/esterification of alcohols and amines/acids with high resistance and low reactivity, with the activity of about 104~106 times that of pyridine. Acyl transfer is a common transformation in nature and organic synthesis, in which chiral DMAP is a common asymmetric acyl transfer catalyst.
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4-Dimethylaminopyridine (DMAP for short), with CAS No. 1122-58-3, chemical formula C₇H₁₀N₂ and molecular weight 122.17, appears as white to pale yellow crystalline powder, easily soluble in organic solvents such as ethanol and acetone, and is an efficient organic catalyst. Its core application is in the field of organic synthesis. As a high-efficiency catalyst for acylation reactions, it can significantly accelerate the acylation reactions of carboxylic acids, acid anhydrides with alcohols and amines, and is widely used in fine chemical fields such as drug synthesis, spice preparation and dye synthesis, greatly improving reaction efficiency and yield. In the medical field, it is used as an intermediate for the synthesis of antibiotics, vitamins, hormones and other drugs, simplifying synthesis steps and reducing production costs. In addition, it is used for polymer material modification, phase transfer catalyst in organic reactions, and reagent in analytical chemistry, and is an indispensable special catalytic raw material in fine chemicals and pharmaceutical synthesis fields.
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