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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298538Generated: October 29, 2026

4,6-Dichloro-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one → HCID 485911, compound

https://huagongshe.com/reaction/2298538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-oneHCID 9882326—
Reactant2-(2,2-Dibromovinyl)furanHCID 10857943—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 485911HCID 485911110.5%

Reaction Steps

To a solution of 5.9 g (25 mmoles) of 1,1-dibromo-2-(furan-2-yl)ethylene in 124 mL of anhydrous THF at −20° was added dropwise 31.0 mL of 1.6 M n-butyllithium in hexanes (50 mmoles). This solution was allowed to warm to ambient temperature over a period of 30 min, after which time it was cooled to −50°. 4,6-Dichloro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one (2.65 g, 9.27 mmoles) was added in one portion, and the resulting solution was allowed to warm to −35° over 40 min. The reaction was quenched by the addition of aqueous ammonium chloride, and this mixture was poured onto water and extracted twice with ethyl acetate. The combined extracts were washed with brine, dried over sodium sulfate, and evaporated. The crude product was purified by column chromatography on silica gel (elution with 15% and 30% ethyl acetate in hexanes) affording 3.5 g of a solid which was recrystallized from ethyl acetate/hexanes to afford 3.03 g (95.7%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492515B2
Source datasetuspto-grants-2002_12
ORD IDord-32ae0db2be664cbfba70854d352627ad
Source noteuspto-grants-2002_12