HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532022Generated: November 2, 2026
Acetamidomalonic acid diethyl ester → HCID 10501146, compound
https://huagongshe.com/reaction/1532022
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | HCID 10635308 | HCID 10635308 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 10501146 | HCID 10501146 | 66.1% |
Reaction Steps
A mixture of diethyl acetamidomalonate (1.6 g, 7.4 mmol) and potassium tert-butoxide (0.9 g, 8.0 mmol) in N-methylpyrrolidone (30 mL) was stirred at room temperature for 30 min. Ethyl 4-(bromomethyl)-3-methoxyisoxazole-5-carboxylate (1.8 g, 6.8 mmol) in N-methylpyrrolidone (10 mL) was added (temp 22-28° C.) and the resulting mixture was stirred at room temperature for 1.5 h. The reaction mixture was poured onto an ice/water mixture (100 mL) and the aqueous phase was extracted with EtOAc (3×150 mL). The organic extracts were washed with an aqueous solution of potassium tert-butoxide, water (100 mL) and brine (100 mL), dried (MgSO4) and concentrated in vacuo. Flash chromatography (silica gel, eluent: EtOAc/heptane=1:1) afforded crude title compound (1.8 g, 66%). A small sample was recrystallized (EtOAc/heptane) to give colourless crystals: mp 78-80° C. The crude product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06200999B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-5b0e4d0de62b40f3884f286a300d088f |
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| Source note | uspto-grants-2001_03 |
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