HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695962Generated: October 25, 2026
Hydrochloric Acid → 3-Isoxazol-5-yl-3-oxo-propionic acid ethyl ester
https://huagongshe.com/reaction/1695962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Isoxazole-5-carbonyl chloride | HCID 2736707 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Isoxazol-5-yl-3-oxo-propionic acid ethyl ester | HCID 59515581 | — |
Reaction Steps
To a stirred solution of diethyl malonate (2.6 ml, 2.74 g) in THF (40 ml) under an atmosphere of nitrogen at −60° C. was added nbutyl lithium (2.5 M, 18.9 ml) dropwise over 15 mins, keeping the temperature constant. The reaction became a cloudy white colour from the formation of the di-lithium salt then became yellowish. After 10 mins, the reaction was cooled to −78° C., when a solution of Isoxazole-5-carbonyl chloride (1 g) in THF (10 ml) was added dropwise over 15 mins. The reaction then warmed to −45° C. and stirred for 1 h, the solution had gone pale brown. The reaction was then poured into 1M HCl solution (50 ml) with stirring and extracted with CH2Cl2 (2×150 ml). The combined organic layers were washed with sat. NaCO3 soln (1×30 ml), dried over MgSO4, filtered and concentrated in vacuo to give the product as a pale oil which was used as such in the next step. Yield 1.1 g, 35.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163757B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-888347d63b5a497da5dc8b14e36b0edf |
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| Source note | uspto-grants-2012_04 |
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