HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Nitroindole → 7-Aminoindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Nitroindole | HCID 23396 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 7-Aminoindole | HCID 111634 | 96.7% |
Reaction Steps
Charge a 3-gal autoclave with 7-nitroindole (250 g, 1.542 moles), 2B-3 ethyl alcohol (5.0 L), and 10% Pd/C (50.0 g). Stir at 50 psi H2 for 2 h at <27° C. When the reaction is deemed complete, filter the reactor contents through Celite followed by concentration of the filtrate to dryness to yield 197.0 g (96.7%) of the title compound as purple solid. 1H-NMR(CD3OD, 300 MHz), δ 7.16 (d, 1H), 7.00 (dd, 1H), 6.81 (t, 1H), 6.50 (dd, 1H), 6.37 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728150B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-2b65a1f6cbca443e93aec527e743b57a |
| Source note | uspto-grants-2010_06 |