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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3-(4-Chloro-2-methylbenzofuran-7-yl)-1-methyl-6-trifluoromethyluracil | HCID 23289190 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(3-Bromo-4-chloro-2-methylbenzofuran-7-yl)-1-methyl-6-trifluoromethyluracil | HCID 23289193 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06130187 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-b0f9de72a779419e93b7bb6b702f494b |
|---|
| Source note | uspto-grants-2000_10 |
|---|