HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Cyclohexylmethyl-(2-nitro-4-phenoxy-phenyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyclohexanemethylamine | HCID 76688 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Chloro-2-nitro-4-phenoxybenzene | HCID 21937801 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Cyclohexylmethyl-(2-nitro-4-phenoxy-phenyl)-amine | HCID 21937664 | 65.6% |
Reaction Steps
A solution of 1-chloro-2-nitro-4-phenoxy-benzene (0.60 g, 2.58 mmol), (aminomethyl)cyclohexane (1.0 mL, 7.76 mmol) and N,N′-diisopropylethylamine (1.36, 7.76 mmol) in DMF (20.00 mL) was stirred at 100° C. under an inert atmosphere for 18.5 h. The reaction mixture was transferred to a separatory funnel containing HCl (2.0 N). The aqueous layer was extracted with EtOAc and the combined organic layers were washed with water, brine and dried over MgSO4. The solution was filtered through diatomaceous earth and the solvent was evaporated. The resulting dark red residue was flash chromatographed (10% EtOAc/hexane) to give cyclohexylmethyl-(2-nitro-4-phenoxy-phenyl)-amine as a dark red solid (0.55 g, 65.6% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115644B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-68d50fd329664e7592593e61bde894de |
| Source note | uspto-grants-2006_10 |