HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(4-Aminomethylbenzyl)-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-(4-Azidomethylbenzyl)-nitrobenzene | HCID 21877004 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Aminomethylbenzyl)-nitrobenzene | HCID 21876731 | 79% |
Reaction Steps
A solution of 4-(4-azidomethylbenzyl)-nitrobenzene (5.835 g) in tetrahydrofuran (175 mL) was treated with water (0.43 mL) and triphenylphosphine (6.45 g, 1.1 eg). The mixture was stirred at room temperature for 18 hours, and the solvent was evaporated. The residue was suspended in water, and suspension made acidic by the dropwise addition of hydrochloric acid to about pH 1, then extracted with diethyl ether (3×). The aqueous phase was made alkaline with 50% aqueous sodium hydroxide, extracted with dichloromethane (3×) to afford a crude brown oil (5.66 g). Chromatography on silica gel, eluting with dichloromethane/methanol/ammonium hydroxide, gave 4-(4-aminomethylbenzyl)-nitrobenzene (3.91 g, 79%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07141584B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-90c9b7e726284b54835a440f4ce5004e |
| Source note | uspto-grants-2006_11 |