HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-tert-butyl-2,4-dinitrobenzene → 4-(Tert-butyl)-3-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-tert-butyl-2,4-dinitrobenzene | HCID 238590 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(Tert-butyl)-3-nitroaniline | HCID 316163 | — |
Reaction Steps
A mixture of 1,3-dinitro-4-tert-butylbenzene (10.0 g) in H2O (56 ml) was heated to reflux. A mixture of Na2S (21.42 g) and sulfur (2.85 g) in H2O (34 ml) was added over 1 h via an addition funnel. The reaction maintained at reflux for 1.5 h then cooled to RT and extracted with EtOAc. The organic extracts were combined and washed with H2O, brine, dried over MgSO4 and concentrated in vacuo to afford 4-tert-butyl-3-nitro-phenylamine which was used as is without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06878714B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-ff86e69152384868a7a4248393b2e3e1 |
| Source note | uspto-grants-2005_04 |