Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1-Chloro-2,4,6-trifluorobenzene | HCID 2736662 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Chloro-3,5-difluoroaniline | HCID 2736494 | — |
Reaction Steps
33.4 g of 2-chloro-1,3,5-trifluorobenzene and 200 ml of methanol saturated with ammonia gas at room temperature were sealed in a Teflon-coating autoclave and heated on an oil bath at 160° C. for 40 hours. After the reaction, the solvent and unreacted 2-chloro-1,3,5-trifluorobenzene were distilled off from the reaction mixture under reduced pressure, and the remaining mixture of a solid component and an oily component was extracted with ether to obtain an oily product in an amount of 31.7 g (yield of 2-chloro-3,5-difluoroaniline: 95% determined by GLC analysis).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05510533 |
|---|
| Source dataset | uspto-grants-1996_04 |
|---|
| ORD ID | ord-d424f3780d6b4a0bb5f422de7801efe8 |
|---|
| Source note | uspto-grants-1996_04 |
|---|