HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-amino-4-bromo-N-(4-bromo-2-fluorobenzyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-bromo-N-(4-bromo-2-fluorobenzyl)-2-nitrobenzamide | HCID 14458987 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-amino-4-bromo-N-(4-bromo-2-fluorobenzyl)benzamide | HCID 14458995 | 98% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A mixture of 4-bromo-N-(4-bromo-2-fluorobenzyl)-2-nitrobenzamide (3.4 g) and iron (1.45 g) in acetic acid (66 ml) was stirred at 100° C. for 30 minutes. After cooling, iron was filtered off. The filtrate was evaporated to give a residue, which was made alkaline with aqueous 1N sodium hydroxide and extracted with ethyl acetate. The extract was washed with water and dried. Removal of the solvent gave 2-amino-4-bromo-N-(4-bromo-2-fluorobenzyl)benzamide (3.10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04883800 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-4eea3f8d26614eabaecd02eb0fccda4f |
| Source note | uspto-grants-1989_11 |