HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 8-Bromo-5-isopropoxy-quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Isopropoxyquinoline | HCID 58550862 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 8-Bromo-5-isopropoxy-quinoline | HCID 58550976 | 92% |
Reaction Steps
To a solution of 5-isopropoxyquinoline (1.87 g, 10.0 mmol) in acetonitrile (100 mL) was added NBS (1.78 g, 10.0 mmol) at 0° C. The mixture was stirred at rt for 2 h before the solvent was removed. The residue was partitioned between EtOAc and H2O. The layers were separated and the organic layer was washed with brine, dried over MgSO4, and concentrated. The crude material was purified by column chromatography (0-10% EtOAc-Hex) to provide 8-bromo-5-isopropoxy-quinoline (92%) as a light brown solid. ESI-MS m/z calc 265.1. found 266.1 (M+1)+. Retention time: 1.44 minutes (3 min run).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598164B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-d2dfd788fe3846daaeb977ef0b2acde1 |
| Source note | uspto-grants-2013_12 |