HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 2-Chloro-4-methyl-quinolin-6-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-Chloro-6-methoxy-4-methylquinoline | HCID 224788 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-4-methyl-quinolin-6-ol | HCID 766382 | 80.4% |
Reaction Steps
A solution of 2-chloro-6-methoxy-4-methylquinoline (0.20 g) in dichloromethane (15 mL) was cooled to −78° C., followed by addition of a solution (5.3 mL) of 1 M boron tribromide in dichloromethane, and the mixture was stirred for 12 h while slowly heating to room temperature. To the reaction mixture was added a saturated sodium hydrogencarbonate solution to make it basic, and the mixture was extracted with chloroform. The aqueous layer was reextracted with a mixture solution of ethyl acetate and n-butanol, then the organic layer was combined and concentrated under reduced pressure, and the resulting solids were washed with diethyl ether to obtain 2-chloro-6-hydroxy-4-methylquinoline (0.15 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044068B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-a3f835033b6041bb9711c03341fcb6e9 |
| Source note | uspto-grants-2011_10 |