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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(4-Chloro-2-methoxyphenyl)-1-methyl-6-trifluoromethyluracil | HCID 23289192 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Chloro-2-hydroxyphenyl-1-methyl-6-trifluoromethyluracil | HCID 23289173 | 70.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06130187 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-cbdab467ea984eeb85ceb942bea05958 |
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| Source note | uspto-grants-2000_10 |
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