HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → 2,4,5-Trifluoro-3-methoxyaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-(3-Methoxy-2,4,5-trifluorophenyl)-phthalimide | HCID 20067133 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,4,5-Trifluoro-3-methoxyaniline | HCID 2775277 | 85.5% |
Reaction Steps
1.1 g (0.02 mole) of hydrazine hydrate was added to a suspension of 2.15 g (0.007 mole) of N-(3-methoxy-2,4,5-trifluorophenyl)phthalimide (XXXVI) [prepared as described in Step (F3) above] in 30 ml of ethanol, and the mixture was heated under reflux with stirring for 2 hours. The reaction mixture was cooled to room temperature and then filtered. The filtrate was concentrated by evaporation under reduced pressure, and the residue was dissolved in toluene. The resulting solution was washed with water and dried, and the solvent was then removed by evaporation under reduced pressure to afford 1.06 g of 3-methoxy-2,4,5-trifluoroaniline (XXIII) as pale brown needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04997943 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-4e78f93e281f4646b98739d707826e81 |
| Source note | uspto-grants-1991_03 |