HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Dimethyl 2-methyl-3-hydroxy-6-vinylpyridine 4,5-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Dimethyl maleate | HCID 5271565 | — |
| Reactant | 5-Ethoxy-4-methyl-2-vinyloxazole | HCID 20263981 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Dimethyl 2-methyl-3-hydroxy-6-vinylpyridine 4,5-dicarboxylate | HCID 20263984 | — |
Reaction Steps
A mixture of 0.2 mole of dimethyl maleate and 0.1 mole of 5-ethoxy-4-methyl-2-vinyloxazole are heated at 110°-115° C. for 4 hours. The reaction mixture is cooled and 20 ml. of a 25% solution of hydrogen chloride (dry) in absolute methanol added. Addition of ether to the cooled reaction mixture precipitates the hydrochloride salt of the product. The free base is obtained by dissolving the hydrochloride salt in a minimum volume of water, adding solid sodium bicarbonate to pH 6.5 to 7.0 and extracting with chloroform. The combined chloroform extracts are dried over sodium sulfate and concentrated in vacuo to give dimethyl 2-methyl-3-hydroxy-6-vinyl-pyridine 4,5-dicarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04053606 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-7231c0c7b7f5483c9790c01e0b2eba79 |
| Source note | uspto-grants-1977_10 |