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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366337Generated: October 29, 2026

Water → 3-(3-Bromo-4-chloro-2-methylbenzofuran-7-yl)-1-methyl-6-trifluoromethyluracil

https://huagongshe.com/reaction/366337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromineHCID 24408—
Reactant3-(4-Chloro-2-methylbenzofuran-7-yl)-1-methyl-6-trifluoromethyluracilHCID 23289190—
SolventAcetic AcidHCID 176—
Product3-(3-Bromo-4-chloro-2-methylbenzofuran-7-yl)-1-methyl-6-trifluoromethyluracilHCID 2328919350%

Reaction Steps

1.0 g (2.8 mmol) of 3-(4-chloro-2-methylbenzofuran-7-yl)-1-methyl-6-trifluoromethyluracil was dissolved in 30 ml of acetic acid, and 0.9 g (5.6 mmol) of bromine was dropwise added thereto at room temperature. After completion of the dropwise addition, stirring was carried out at 40° C. for 6 hours. After completion of the reaction, the reaction solution was poured into water and extracted with ethyl acetate. The organic layer was washed sequentially with water and 10% aqueous ammonia and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. Then, the obtained residue was purified by silica gel column chromatography to obtain 0.6 g (yield: 50.0%) of a pale yellow glassy substance. Refractive index: 1.5632 (20° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130187
Source datasetuspto-grants-2000_10
ORD IDord-b0f9de72a779419e93b7bb6b702f494b
Source noteuspto-grants-2000_10