HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-phenyl-1H-indol-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 3-Nitroso-2-phenyl-1H-indole | HCID 343976 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-phenyl-1H-indol-3-amine | HCID 2749340 | — |
Reaction Steps
To a solution of 3-nitroso-2-phenyl indole (28) (25 gm, 0.129 mol) in ethanol (450 ml) was added 2N sodium hydroxide (300 mL, 5.0 eq) followed by sodium dithionite (38 g). The reaction was heated at reflux for 5 h, then filtered. The solid was washed with water and dried under vacuum to provide Compound 29 as a yellow solid. Yield=15 g (72.1%). ES-MS: 209.25 (M++1); NMR (DMSO-d6): δ 7.0 (m, 1H), 7.1 (m, 1H), 7.22 (m, 1H), 7.32 (m, 2H), 7.40 (m, 1H), 7.48 (m, 2H), 7.60 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956035B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-f14dd1e60a094d33ba7aff9f0ba1e021 |
| Source note | uspto-grants-2005_10 |