HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(2-Aminobenzyl)-6-phenyl-[1,3]-oxazinan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-(2-Nitrobenzyl)-6-phenyl-[1,3]-oxazinan-2-one | HCID 67459520 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(2-Aminobenzyl)-6-phenyl-[1,3]-oxazinan-2-one | HCID 67462016 | 99.3% |
Reaction Steps
3-(2-Nitrobenzyl)-6-phenyl-[1,3]-oxazinan-2-one (1.59 g, 5.10 mmol), iron powder (1.42 g, 25.4 mmol), ammonium chloride (0.14 g, 2.62 mmol) were suspended in ethanol (30 ml) and water (15 ml) and heated to reflux for 1.5 hours. After cooling to room temperature, the reaction mixture was filtered with suction and extracted with ethyl acetate. The organic layer was washed with a saturated brine and then dried over anhydrous sodium sulfate, and 3-(2-aminobenzyl)-6-phenyl-[1,3]-oxazinan-2-one (1.43 g) was obtained by evaporating the solvent under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048825B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-279427bedc5d4d239b00cc6dfc2c8131 |
| Source note | uspto-grants-2011_11 |