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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440690Generated: October 29, 2026

Ethyl Acetate → 3-(5-chloro-3,4-dihydro-7-fluoro-2H-1-benzopyran-8-yl)-6-trifluoromethyluracil

https://huagongshe.com/reaction/440690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-amino-4,4,4-trifluorocrotonateHCID 5702529—
Reactant5-chloro-3,4-dihydro-7-fluoro-2H-1-benzopyran-8-yl isocyanateHCID 22404728—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-(5-chloro-3,4-dihydro-7-fluoro-2H-1-benzopyran-8-yl)-6-trifluoromethyluracilHCID 22404800—

Reaction Steps

By a method analogous to that of Example 1, Step G, 2.5 grams (0.011 mole) of 5-chloro-3,4-dihydro-7-fluoro-2H-1-benzopyran-8-yl isocyanate was reacted with ethyl 3-amino-4,4,4-trifluorocrotonate and 0.66 gram (0.012 mole) of sodium hydride (60% in mineral oil) in 150 mL of tetrahydrofuran. The crude reaction product was subjected to column chromatography on silica gel, with 1:2 ethyl acetate:hexane as the eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding 3.0 grams of 3-(5-chloro-3,4-dihydro-7-fluoro-2H-1-benzopyran-8-yl)-6-trifluoromethyluracil. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521147
Source datasetuspto-grants-1996_05
ORD IDord-c72d9c88583f4d8fb00bdd567fcfeee9
Source noteuspto-grants-1996_05