HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242066Generated: October 25, 2026
Ethyl oxoacetate → Ethyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylate
https://huagongshe.com/reaction/1242066
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | 1-Methoxy-3-trimethylsilyloxy-1,3-butadiene | HCID 101051 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylate | HCID 22495097 | 75% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115624B1 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-c3730e9cff94473b822c79093dd8dd0b |
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| Source note | uspto-grants-2006_10 |
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