Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethyl maleate | HCID 5271565 | — |
| Reactant | HCID 68644161 | HCID 68644161 | — |
| Product | HCID 58636771 | HCID 58636771 | 66% |
Reaction Steps
2-Cyclopropyl-5-ethoxy-4-methyl-oxazole (164) (33.8 g, 0202 mmol) in neat dimethyl maleate (115.8 g, 807 mmol) was refluxed for 4 hours. The reaction was cooled to 0° C., added anhydrous methyl alcohol (500 mL) and bubbled hydrogen chloride gas into the suspension for 15 minutes. The reaction flask was sealed with a rubber septum and kept in a fridge for overnight. The solid was filtered off and washed with methanol and diethyl ether. The filtrate was evaporated to give 2-cyclopropyl-5-hydroxy-6-methyl-pyridine-3,4-dicarboxylic acid dimethyl ester (165) (35.2 g, 66% yield) as a colorless solids.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812037B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-f088b2b84f014b26863df0b98aebacbe |
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| Source note | uspto-grants-2010_10 |
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