HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-Fluoroquinolin-7-OL
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 3-Fluoro-7-methoxyquinoline | HCID 22030856 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Fluoroquinolin-7-OL | HCID 135763124 | — |
Reaction Steps
3-Fluoro-7-methoxyquinoline (130 mg, 0.74 mmol) was taken up in dichloromethane (2 ml) under nitrogen and treated with boron tribromide (4 ml of a 11.0M solution of in dichloromethane). The reaction mixture was stirred for 24 hours at ambient temperature followed by quenching the reaction by the slow addition of excess methanol. The solution was stirred for a further 2 hours and evaporated to dryness to give 3-fluoro-7-hydroxyquinoline which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074800B1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-76e7e2024c9c4fb4b22242708b9a260b |
| Source note | uspto-grants-2006_07 |