HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → (1H-Indol-7-YL)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Indole-7-carboxaldehyde | HCID 2734629 | — |
| Catalyst | Ammonium Hydroxide | HCID 14923 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | (1H-Indol-7-YL)methanamine | HCID 21950026 | 89% |
Reaction Steps
Add hydroxylamine hydrochloride (2.87 g, 41.37 mmol) and ammonium acetate (4.78 g, 62.06 mmol) to a solution of indole-7-carboxaldehyde (3.0 g, 20.68 mmol) in ethanol: H2O (3:1) (120 ml). Stir at room temperature for 2 hours. Add ammonium hydroxide (25 ml, 0.72 mmol) and zinc (11.0 g, 8.1 mmol) in portions. Filter the reaction mixture, dilute with ethyl acetate, and wash with water. Extract the organic layer with 1N HCl. Make the aqueous layer basic by adding 1N NaOH and extract with ethyl acetate. Wash the organic layer with water followed by saturated aqueous sodium chloride, dry over magnesium sulfate, and concentrate under reduced pressure to provide the desired compound (2.69 g, 89%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022065B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-9fae0dbc2cb240518c26b72effea50fb |
| Source note | uspto-grants-2011_09 |