HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → HCID 135515429, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 10354455 | HCID 10354455 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | HCID 135515429 | HCID 135515429 | 24.4% |
Reaction Steps
2-Amino-6-benzylamino-3-nitropyridine (25 g, 0.10 mol) was hydrogenated under 5.5 bar of H2 in the presence of 10 g of Raney-Ni in 400 mL of dioxane at 60 C. After 2 hours the reaction mixture was cooled to room temperature, filtrated and 4-hydroxy phenylglyoxal was added and stirred for 2 hours under an argon atmosphere. The suspension was then diluted with water, the solid was collected by filtration, washed with water, recrystallized from 2-propanol, and dried at 50 C. in vacuo to give 6-benzylamino-3-(4-hydroxyphenyl)-5-azaquinoxaline (8 g, 24.4%, m.p. 271-273 C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06180631B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-c1661d116d23443cb80b215130a28d7d |
| Source note | uspto-grants-2001_01 |