Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl Acetate | HCID 6584 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 4-methyl-1,2-oxazole-3-carboxylate | HCID 14676600 | — |
| Product | HCID 20029387 | HCID 20029387 | — |
Reaction Steps
A solution of 2.8 g of 2B in 5.4 ml of methyl acetate was added to 1 g of sodium hyride, and the mixture was heated at reflux for 7 hours, then 0.25 ml of methanol was added. When gas evolution ended, the mixture was heated at reflux for 15 minutes, then cooled and stirred at room temperature overnight. The mixture was quenched in water, the resulting mixture was acidified with glacial acetic acid, and extracted with methylene chloride. The extract was dried (MgSO4) and stripped of solvent. The residue was chromatographed on silica gel with a 1:3 v:v mixture of ethyl acetate and hexane as eluent. The middle fractions that were obtained gave ethyl 3-(4-methyl-3-isoxazolyl)-3-oxopropionate (2C), as a light yellow oil. 27 g of sodium methoxide was dissolved in a mixture of 100 ml of methanol and 100 ml of THF. 50 grams of aluminum oxide (activated, neutral, Brockmann I, Aldrich) was added and the mixture was stirred for 30 minutes. The solvents were removed under reduced pressure to give aluminum oxide-supported sodium-methoxide (2D).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853027 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-c8b29cf6c3e245bd875f8fb6a28076b2 |
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| Source note | uspto-grants-1989_08 |
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