HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycerol → 7-Bromo-5-fluoroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycerol | HCID 753 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | 3-Bromo-5-fluoroaniline hydrochloride | HCID 46738075 | — |
| Catalyst | Ferrous sulfate heptahydrate | HCID 62662 | — |
| Product | 7-Bromo-5-fluoroquinoline | HCID 66600385 | 30% |
| Product | 5-Bromo-7-fluoroquinoline | HCID 68755221 | — |
Reaction Steps
To 3-bromo-5-fluoroaniline hydrochloride (2.9 g, 12.89 mmol) was added glycerol (1.9 mL, 25.99 mmol), nitrobenzene (1.3 mL), sulfuric acid (3.5 mL) and iron (II) sulfate heptahydrate (0.23 g, 0.82 mmol). The reaction mixture was placed in an oil bath set at 80° C. and stirred overnight followed by basification with 12N NaOH and extraction with dichloromethane. The organic phase was collected, dried (sodium sulfate), filtered and concentrated under reduced pressure. Purification by flash chromatography (silica, 50:50 ethyl acetate/hexane) gave 5-bromo-7-fluoroquinoline and 7-bromo-5-fluoroquinoline (1.03 g, 30%) Retention time (min)=1.877 and 1.967, method [4], MS (ESI) 227.9 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450363B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-bda02299821f4c7ebc79df901c249226 |
| Source note | uspto-grants-2013_05 |