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| | Diethyl pyridine-2,3-dicarboxylate Basic information |
| Product Name: | Diethyl pyridine-2,3-dicarboxylate | | Synonyms: | DIETHYL 2,3-PYRIDINEDICARBOXYLATE;Diethyl pyridine-2,3-dicarboxylate;2,3-Pyridinedicarboxylic acid diethyl ester;Diethyl 2,3-quinolinate;Diethyl 3,4-pyridinecarboxylate;2,3-diethyl pyridine-2,3-dicarboxylate;2,3-Bis(ethoxycarbonyl)pyridine;2,3-Pyridinedicarboxylic acid, 2,3-diethyl ester | | CAS: | 2050-22-8 | | MF: | C11H13NO4 | | MW: | 223.23 | | EINECS: | | | Product Categories: | | | Mol File: | 2050-22-8.mol |  |
| | Diethyl pyridine-2,3-dicarboxylate Chemical Properties |
| Boiling point | 282 °C | | density | 1.165±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | solubility | DMSO (Slightly), Methanol (Slightly) | | pka | -0.55±0.10(Predicted) | | form | Oil | | color | Light Yellow to Yellow |
| Hazard Codes | Xi | | HazardClass | IRRITANT | | HS Code | 2933399990 |
| | Diethyl pyridine-2,3-dicarboxylate Usage And Synthesis |
| Uses | Diethyl Pyridine-2,3-dicarboxylate is a useful reagent in preparation of herbicides. | | Synthesis | Example 1, Synthesis of diethyl pyridine-2,3-dicarboxylate: alkyne propylamine (0.2 mmol), diethyl butynedioate (34 g, 0.2 mmol) and ethanol (100 mL) were added to a 250 mL reaction flask, and 50% hydrogen peroxide (~26 mL, 0.30 mmol) was added with stirring. The reaction mixture was heated to 65 °C and kept for 12 h. The progress of the reaction was monitored by TLC (unfolding agent: petroleum ether/ethyl acetate = 2:1, v/v) until the complete disappearance of diethyl butynedioate. After completion of the reaction, ethanol was recovered by atmospheric distillation. Water (100 mL) was added to the residue and the mixture was extracted with ethyl acetate (50 mL x 3). The organic layer (upper layer) was combined and washed sequentially with water (50 mL) and saturated brine (50 mL). After recovery of ethyl acetate by atmospheric distillation, a reduced pressure distillation (6 mmHg) was carried out and the fraction at 165-170 °C/6 mmHg was collected to give diethyl pyridine-2,3-dicarboxylate (36.6 g, 82% yield). | | References | [1] Patent: CN104447528, 2016, B. Location in patent: Paragraph 0026; 0027 |
| | Diethyl pyridine-2,3-dicarboxylate Preparation Products And Raw materials |
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