HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 2-(Benzylamino)-4-(3-diethylamino-1-propoxy)nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 2-Fluoro-4-(3-diethylamino-1-propoxy)nitrobenzene | HCID 22014733 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Benzylamino)-4-(3-diethylamino-1-propoxy)nitrobenzene | HCID 22014715 | 86.7% |
Reaction Steps
A solution of 2-fluoro-4-(3-diethylamino-1-propoxy)nitrobenzene (2 mmol; preparation described in Example 5) in THF (5 mL) is treated with benzylamine (2.4 mmol) at rt. After completion of the reaction, the reaction mixture is concentrated in vacuo. The residue is redissolved in EtOAc (10 mL), washed with saturated sodium bicarbonate solution, water, and brine. The organic phase is then dried over sodium sulfate and the solvent is removed in vacuo to afford the product, 2-(benzylamino)-4-(3-diethylamino-1-propoxy)nitrobenzene (620 mg) which was used for further transformation without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087632B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-af39e966e26540f5ac091befab22f4c6 |
| Source note | uspto-grants-2006_08 |