HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → 3-Fluoroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 3-Aminoquinoline | HCID 11375 | — |
| Solvent | 1,4-Dichlorobenzene | HCID 4685 | — |
| Product | 3-Fluoroquinoline | HCID 96405 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
Tert-butylnitrite (4.6 ml, 38.7 mmol) was added dropwise over 15 min to a solution of quinolin-3-amine (4.61 g, 32.0 mmol) and borontrifluoride-etherate (6 ml, 47.3 mmol) in dichlorobenzene (100 ml). The solution was heated to 100° C. After stirring for 1 h, the solution was cooled to ambient temperature and the dichlorobenzene was decanted leaving 3-fluoroquinoline as a black residue. Method [8] retention time 3.28 min by HPLC (M+ 148).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450363B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-8eed76372bb54e98bbf189045894b89d |
| Source note | uspto-grants-2013_05 |