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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidomalonic acid diethyl esterHCID 14041—
ReactantHCID 10635308HCID 10635308—
ReactantPotassium tert-butoxideHCID 23665647—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 10501146HCID 1050114666.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200999B1
Source datasetuspto-grants-2001_03
ORD IDord-5b0e4d0de62b40f3884f286a300d088f
Source noteuspto-grants-2001_03