HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Amino-4-bromobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Bromo-2-nitrobenzaldehyde | HCID 608099 | — |
| Catalyst | Ferrous sulfate heptahydrate | HCID 62662 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-4-bromobenzaldehyde | HCID 17914598 | 89.7% |
Reaction Steps
16.1 ml of an aqueous 29% ammonia solution was added to a mixture of 5.0 g of 2-nitro-4-bromobenzaldehyde, 60.4 g of iron (II) sulfate heptahydrate, 200 ml of methanol, 100 ml of water and 335 μl of concentrated hydrochloric acid in an oil bath kept at 90° C., followed by heating under stirring for 10 minutes. After cooling as it was, insoluble matters were filtered through Celite and the filtrate was extracted with ethyl acetate. The organic phase was washed with brine and the solvent was removed, to give 3.9 g of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06599917B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-551f79048f014245b49e52d82c0e8fd6 |
| Source note | uspto-grants-2003_07 |