Identification | Back Directory | [Name]
dimethyl pyridine-3,5-dicarboxylate | [CAS]
4591-55-3 | [Synonyms]
5-dicarboxylate dimethyl pyridine-3 pyridine-3,5-dicarboxyL Dimethyl 3,5-Pyridinedicarboxylate dimethyl pyridine-3,5-dicarboxylate 3,5-Pyridinedicarboxylic acid dimethyl ester 3,5-Pyridinedicarboxylicacid, 3,5-diMethyl ester | [EINECS(EC#)]
224-981-1 | [Molecular Formula]
C9H9NO4 | [MDL Number]
MFCD00518827 | [MOL File]
4591-55-3.mol | [Molecular Weight]
195.172 |
Chemical Properties | Back Directory | [Melting point ]
84-85 °C | [Boiling point ]
267.6±20.0 °C(Predicted) | [density ]
1.231±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Room Temperature | [solubility ]
Chloroform, Dichloromethane, Methanol | [form ]
Solid | [pka]
1.16±0.20(Predicted) | [color ]
Pale Yellow |
Hazard Information | Back Directory | [Chemical Properties]
Pale Yellow Solid | [Uses]
Dimethyl 3,5-Pyridinedicarboxylate (cas# 4591-55-3) is a compound useful in organic synthesis. | [Synthesis]
The general procedure for the synthesis of methyl 3,5-pyridinedicarboxylate from methanol and 3,5-pyridinedicarboxylic acid is as follows: 3,5-pyridinedicarboxylic acid (5.00 g, 29.92 mmol) was dissolved in methanol (100 ml), concentrated sulfuric acid (2 ml) was added slowly as a catalyst, and the reaction mixture was stirred for 18 hrs under reflux conditions. After completion of the reaction, the solvent methanol was removed by distillation under reduced pressure. Subsequently, the reaction mixture was neutralized with aqueous sodium bicarbonate and separated by extraction with dichloromethane. The dichloromethane layer was collected and washed with saturated aqueous sodium chloride solution to remove residual water-soluble impurities. Eventually, the dichloromethane layer was concentrated by decompression to give the white solid product methyl 3,5-pyridinedicarboxylate (5.5 g, 94% yield). | [References]
[1] ACS Medicinal Chemistry Letters, 2016, vol. 7, # 10, p. 933 - 938 [2] Patent: KR2018/9249, 2018, A. Location in patent: Paragraph 0250; 0251 [3] Angewandte Chemie - International Edition, 2004, vol. 43, # 30, p. 3914 - 3918 [4] Bulletin of the Korean Chemical Society, 2015, vol. 36, # 9, p. 2397 - 2400 [5] Life Sciences, 2005, vol. 78, # 5, p. 495 - 505 |
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