HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402635Generated: November 1, 2026
2-Methoxyethanol → HCID 86708329, compound
https://huagongshe.com/reaction/402635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyethanol | HCID 8019 | — |
| Reactant | Methyl 4-chloroacetoacetate | HCID 36240 | — |
| Reactant | 4-Fluorophenyl isocyanate | HCID 70955 | — |
| Reactant | HCID 86708321 | HCID 86708321 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86708329 | HCID 86708329 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742113B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-91aa5ecd0d80442690412c7b651a85d8 |
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| Source note | uspto-grants-2014_06 |
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