HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387181Generated: October 30, 2026
2-Bromo-6-fluoroaniline → 1-(2-Bromo-6-fluorophenyl)-3-(2-methoxy-5-(trifluoromethyl)phenyl)urea
https://huagongshe.com/reaction/387181
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-6-fluoroaniline | HCID 2782940 | — |
| Reactant | Benzene, 2-isocyanato-1-methoxy-4-(trifluoromethyl)- | HCID 11983909 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | 1-(2-Bromo-6-fluorophenyl)-3-(2-methoxy-5-(trifluoromethyl)phenyl)urea | HCID 57857530 | 87.4% |
Reaction Steps
2-Methoxy-5-trifluoromethylphenyl isocyanate (1.19 kg) is fused at about 35° C. and dissolved in acetonitrile (4.2 l), then 2-bromo-6-fluoroaniline (870 g) is added and rinsed out with acetonitrile (380 ml). The resulting clear solution is stirred at 74-88° C. for 45 h, then concentrated in vacuo (200 mbar) at 50° C. to give a viscous magma (amount of distillate 4.4 l). This is diluted at room temperature with diisopropyl ether (1.5 l), filtered off with suction, washed with diisopropyl ether (1.15 l) and dried at 45° C. in the VDO using entraining nitrogen to constant mass (24 h). A total of 1.63 kg of N-(2-bromo-6-fluorophenyl)-N′-[2-methoxy-5-(trifluoromethyl)phenyl]urea is obtained as a solid, corresponding to 87.5% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08372972B2 |
|---|
| Source dataset | uspto-grants-2013_02 |
|---|
| ORD ID | ord-205c67d956684c8db8c57b7dd87c2709 |
|---|
| Source note | uspto-grants-2013_02 |
|---|