HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1242066Erstellt: 26. Oktober 2026
Ethyl oxoacetate → Ethyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylate
https://huagongshe.com/reaction/1242066
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl oxoacetate | HCID 70211 | — |
| Edukt | 1-Methoxy-3-trimethylsilyloxy-1,3-butadiene | HCID 101051 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | Ethyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylate | HCID 22495097 | 75% |
Reaktionsschritte
A solution of glyoxylic acid ethyl ester, polymer form (2.02 g, 8.9 mmol) and (3-methoxy-1-methylene-allyloxy)-trimethyl-silane (1.9 ml, 8.9 mmol, Danishefsky's diene) in benzene (12 ml) was placed under nitrogen. Zinc chloride (0.5N in tetrahydrofuran, 8.9 ml, 4.45 mmol) was added and the reaction stirred at ambient temperature for 72 h. The mixture was concentrated in vacuo, diluted with ethyl acetate (100 ml) and washed with 1 N hydrochloric acid (20 ml), saturated sodium bicarbonate (20 ml), and brine (20 ml). The organic layer was dried (Na2SO4), filtered, and the solvent evaporated in vacuo. The residue was purified by silica gel chromatography using a mixture of ethyl acetate/hexane (1:2) as eluant. Pure fractions were collected and the solvent evaporated in vacuo which afforded 1.2 g (75%) of 4-oxo-3,4-dihydro-2H-pyran-2-carboxylic acid ethyl ester as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07115624B1 |
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| Quelldatensatz | uspto-grants-2006_10 |
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| ORD ID | ord-c3730e9cff94473b822c79093dd8dd0b |
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| Quellennotiz | uspto-grants-2006_10 |
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