HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 2-(7-hydroxyquinolin-4-yloxy)acetic Acid Hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-(7-Methoxyquinolin-4-yloxy)acetic acid | HCID 57691021 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(7-hydroxyquinolin-4-yloxy)acetic Acid Hydrobromide | HCID 136330124 | 139.8% |
Reaction Steps
To a pressure vial was added 2-(7-methoxyquinolin-4-yloxy)acetic acid (1.00 g, 4.29 mmol) in DCE (0.6 M, 7 mL). The vial was cooled in an ice bath and to the solution was added BBr3 (1.62 ml, 17.2 mmol). The reaction was allowed to warm to room temperature and stirred overnight. While some starting material remained, the reaction was stopped and diluted with DCM (keep in hood due to fuming). The solids were filtered and dried over high vacuum to yield a light brown crude solid (˜1.8 g). The material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198448B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-39dda22102f24e7daa033420728d9aa9 |
| Source note | uspto-grants-2012_06 |