HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoroaniline → 4-Bromo-2-fluoroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoroaniline | HCID 9584 | — |
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | Bromine | HCID 24408 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Fluorobenzene | HCID 10008 | — |
| Product | 4-Bromo-2-fluoroaniline | HCID 123050 | — |
Reaction Steps
In a suitable aprotic solvent (e.g., CH2Cl2, toluene, fluorobenzene, or the like) 1 mole of tetrabutylammonium bromide is dissolved and stirred as 1 mole of Br2 (bromine) is added. This mixture of tetrabutylammonium trihalide and solvent is cooled to 10° before 1 mole of 2-fluoroaniline or 4-fluoroanilin, or a mixture of both, is added. The reaction takes place immediately to produce 4-bromo-2-fluoroaniline.HBr, or 2-bromo-4-fluoroaniline.HBr, or a mixture of the two. The salt is then collected and dried before carrying it up to the next step. Catalyst and solvent are recovered for recycle.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05157169 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-3cd2bd1330394cf9866198f7366292b2 |
| Source note | uspto-grants-1992_10 |