HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-Fluoro-7-hydroxy-2-methylquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 3-Fluoro-7-methoxy-2-methylquinoline | HCID 22030792 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Fluoro-7-hydroxy-2-methylquinoline | HCID 135763123 | — |
Reaction Steps
3-Fluoro-7-methoxy-2-methylquinoline (0.16 g, 0.85 mmol) was taken up in dichloromethane (4 ml) under nitrogen and treated with boron tribromide solution (4 ml of a 1.0M solution in dichloromethane, 4.0 mmol). The reaction was stirred for 24 hours at ambient temperature followed by the slow addition of excess methanol. The solution was stirred for a further 2 hours and then evaporated to dryness to give 3-fluoro-7-hydroxy-2-methylquinoline which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492560B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-1671a113e0e84df59dd109665832c08a |
| Source note | uspto-grants-2013_07 |