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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402635Generated: November 1, 2026

2-Methoxyethanol → HCID 86708329, compound

https://huagongshe.com/reaction/402635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantMethyl 4-chloroacetoacetateHCID 36240—
Reactant4-Fluorophenyl isocyanateHCID 70955—
ReactantHCID 86708321HCID 86708321—
CatalystZincHCID 23994—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86708329HCID 86708329—

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution of methyl 2-[(4-fluorophenyl)amino]-4-oxo-4,5-dihydrofuran-3-carboxylate (0.063 g, 0.25 mmol) which similarly prepared according to the procedure described in the Example 2, First step using methyl 4-chloroacetoacetate and 4-fluorophenyl isocyanate, 2-methoxyethanol (0.2 mL, 2.5 mmol) and zinc cluster catalyst (Zn4(OCOCF3)6O) (0.0048 g, 0.0050 mmol) in anhydrous dioxane (1.0 mL) was stirred with the microwave synthesizer (Biotage Initiator™) at 120° C. for 1 h. Cooled to ambient temperature, the reaction mixture was concentrated under reduced pressure. The residue was purified by chromatography on silica gel(chloroform/ethyl acetate) to afford 2-methoxyethyl 2-[(4-fluorophenyl)amino]-4-oxo-4,5-dihydrofuran-3-carboxylate as solid (0.024 g, y. 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742113B2
Source datasetuspto-grants-2014_06
ORD IDord-91aa5ecd0d80442690412c7b651a85d8
Source noteuspto-grants-2014_06