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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231125Generated: October 25, 2026

Ethyl 4-chloroacetoacetate → Ethyl 2-[[4-(ethoxycarbonyl)phenyl]amino]4,5-dihydro-4-oxo-3-furancarboxylate

https://huagongshe.com/reaction/231125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chloroacetoacetateHCID 69484—
ReactantEthyl 4-isocyanatobenzoateHCID 589805—
SolventTriethylamineHCID 8471—
ProductEthyl 2-[[4-(ethoxycarbonyl)phenyl]amino]4,5-dihydro-4-oxo-3-furancarboxylateHCID 14198527—

Reaction Steps

Triethylamine (9.87 ml) was added dropwise, over a period of 1 hour to a cooled (ice bath) solution of ethyl 4-chloroacetoacetate (9.87 g, 60 mmol) and ethyl p-isocyanatobenzoate (14.34 g, 75 mmol) in 60 ml of petroleum ether-ethyl acetate (10:1 by volume), under nitrogen atmosphere. The reaction mixture was stirred at 0°-5° C. for 1 hour. The resulting ethyl 2-[[4-(ethoxycarbonyl)phenyl]-amino]-4,5-dihydro-4-oxo-3-furancarboxylate was filtered and then washed sequentially with petroleum ether, 1 N hydrochloric acid and water. Yield 13.0 g Mp 152°-153° C. (isopropanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845122
Source datasetuspto-grants-1989_07
ORD IDord-e9bcb238e0b247768e6bd2b4ecf5655d
Source noteuspto-grants-1989_07