HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 5,6,7,8-Tetrahydroquinoxalin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2-Chloro-5,6,7,8-tetrahydroquinoxaline | HCID 22036934 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 5,6,7,8-Tetrahydroquinoxalin-2-amine | HCID 19087118 | — |
Reaction Conditions
| Temperature | 133 °C |
|---|
Reaction Steps
A seated tube containing 2-chloro-5,6,7,8-tetrahydroquinoxaline (1.51 g, 0.009 mol), concentrated NH4OH (10 mL), isopropyl alcohol (30 mL), and copper powder (300 mg) was heated in an oil bath at 133° C. for 20 hours. The cooled mixture was filtered through celite and washed through the filter agent with H2O and hexanes. The layers were separated and the aqueous portion was washed (2×) with hexanes in order to remove unreacted starting material and then extracted with EtOAc (4×). The combined EtOAc extracts were dried over sodium sulfate and concentrated under reduced pressure to yield 2-amino-5,6,7,8-tetrahydroquinoxaline as a yellow-green solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05306819 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-9e0ffffc553747bbbcfafa5ccc4be137 |
| Source note | uspto-grants-1994_04 |