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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366344Generated: October 26, 2026

Boron tribromide → 4-Chloro-2-hydroxyphenyl-1-methyl-6-trifluoromethyluracil

https://huagongshe.com/reaction/366344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(4-Chloro-2-methoxyphenyl)-1-methyl-6-trifluoromethyluracilHCID 23289192—
SolventDichloromethaneHCID 6344—
Product4-Chloro-2-hydroxyphenyl-1-methyl-6-trifluoromethyluracilHCID 2328917370.3%

Reaction Steps

41.0 g (122.5 mmol) of 3-(4-chloro-2-methoxyphenyl)-1-methyl-6-trifluoromethyluracil was dissolved in 1000 ml of dichloromethane, and 470 ml (470.8 mmol) of boron tribromide (1.0M dichloromethane solution) was dropwise added at from -10° C. to -5° C. After stirring at room temperature for 3 hours, the reaction solution was poured into ice water and neutralized with sodium hydrogencarbonate. It was extracted with dichloromethane. The organic layer was washed sequentially with water and a saturated sodium chloride aqueous solution and then, dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. Then, the obtained crude crystals were washed with isopropyl ether to obtain 27.6 g (yield: 70.3%) of the desired product as white crystals. Melting point: 198-202° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130187
Source datasetuspto-grants-2000_10
ORD IDord-cbdab467ea984eeb85ceb942bea05958
Source noteuspto-grants-2000_10