HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 59256698, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 135412675 | HCID 135412675 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59256698 | HCID 59256698 | 47% |
Reaction Steps
A mixture of 6,8-dichloro-3-methylquinoxalin-5-ol (150 mg, 0.655 mmol), benzyl bromide (0.20 mL, 1.68 mmol), KOH (0.09 g) and EtOH (10 mL) was heated under reflux for 16 h, cooled, and concentrated. Dichloromethane (20 mL) was added and the mixture washed with H2O (5 mL×2), dried and concentrated. The residue was purified via SiO2-gel chromatography (dichloromethane/MeOH, 1:0-150:1) to give 8-benzyloxy-5,7-dichloro-2-methylquinoxaline (98 mg, 47%).—1H NMR (CDCl3): δ 8.82 (s, 1H), 7.81 (s, 1H), 7.58 (m, 2H), 7.38 (m, 2H), 5.45 (s, 2H), 2.85 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07692011B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-a0ecb9e73bea402a8bb68527d738a5b6 |
| Source note | uspto-grants-2010_04 |