HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzyl-5-nitroisoindoline → 2-Benzyl-2,3-dihydro-1H-isoindol-5-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzyl-5-nitroisoindoline | HCID 12065977 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Benzyl-2,3-dihydro-1H-isoindol-5-ylamine | HCID 3159244 | 81.6% |
Reaction Steps
4.0 g of 2-benzyl-5-nitroisoindoline prepared in Reference Example 2-(2) was dissolved in 40 ml of methanol and 800 mg of 10% palladium on carbon was added to the solution. The catalytic hydrogenation was performed for 32 hours at room temperature and under atmospheric pressure. After removing the catalyst by filtration, the filtrate was concentrated to obtain 2.88 g of 2-benzyl-5-aminoisoindoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05026856 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-e57fabad950d454c8eee0c892aefd3dc |
| Source note | uspto-grants-1991_06 |