HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 5-Bromo-N,N-bis-(4-methoxy-benzyl)-N''-methyl-benzene-1,2,3-triamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Reactant | 5-Bromo-N,N-bis-(4-methoxy-benzyl)-N'-methyl-2-nitro-benzene-1,3-diamine | HCID 118235376 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 5-Bromo-N,N-bis-(4-methoxy-benzyl)-N''-methyl-benzene-1,2,3-triamine | HCID 118235378 | — |
Reaction Steps
A mixture of 5-Bromo-N,N-bis-(4-methoxy-benzyl)-N′-methyl-2-nitro-benzene-1,3-diamine (170 mmol), NH4Cl (2038 mmol) and Zn (2034 mmol) in 1:1 MeOH/THF (1 L) was stirred at room temperature for 1 h. The mixture was cooled to 0° C. and HCOOH (20 mL) was added slowly. The mixture was allowed to reach room temperature and stirred for 1 h. The mixture was filtered and combined with another one obtained following the procedure described above. The resulting mixture was concentrated. The residue was dissolved in DCM. The organic mixture was washed (sat. NH4Cl), dried (Na2SO4) and concentrated to afford the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440929B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-9fae7736eb804de590a966cb4d8f8bca |
| Source note | uspto-grants-2016_09 |