HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butylamine → N-butyl-5-fluoro-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Difluoronitrobenzene | HCID 67967 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-butyl-5-fluoro-2-nitroaniline | HCID 59566264 | — |
Reaction Steps
To a stirred solution of 2,4-difluoronitrobenzene (50 mmol), Et3N (100 mmol) and DMF (80 mL) was added dropwise a solution of n-butylamine (51 mmol) in DMF (20 mL) at rt, and the mixture was stirred at rt for 5 h. The reaction was quenched by cold H2O (100 mL), and the resulting mixture was extracted with EtOAc (4×100 mL). The combined EtOAc extracts were washed with brine (3×60 mL) and dried (anhydrous Na2SO4). The solvent was removed in vacuo to afford the desired 2-n-butylamino-4-fluoronitrobenzene which was used for further transformation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361678B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-86be9fa1e7da492d91b23a45982dc841 |
| Source note | uspto-grants-2008_04 |