HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N1-(3,5-difluorophenyl)-3,5-difluoro-benzene-1,2-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-(3,5-difluorophenyl)-3,5-difluoro-2-nitroaniline | HCID 67433031 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N1-(3,5-difluorophenyl)-3,5-difluoro-benzene-1,2-diamine | HCID 67433197 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a solution of N-(3,5-difluorophenyl)-3,5-difluoro-2-nitroaniline (1 g, 3.49 mmol) in AcOH (10.5 mL) was added iron powder (585 mg, 10.48 mmol) and the reaction mixture was heated to 100° C. for 1 h. The reaction mixture was cooled to rt and water was added. The organic layer was extracted with EtOAc and was basified by using satd. sodium bicarbonate solution. The organic phase was dried over sodium sulfate and concentrated in vacuo to provide N1-(3,5-difluorophenyl)-3,5-difluoro-benzene-1,2-diamine. The crude product was carried without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575183B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-f8edfff05db04284a8cf60fe69486837 |
| Source note | uspto-grants-2013_11 |