Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 5-Aminoquinoline | HCID 11911 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | Diethylether ethylacetate | HCID 21584169 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Product | 5-Fluoroquinoline | HCID 115243 | 55% |
Reaction Steps
Add sodium nitrite in portions to a suspension of 5-aminoquinoline (50 g, 347 mmol) in 48% HBF4 (200 mL) at 0° C. Stir for 1 hour and then pour into 1:1 diethyl ether/ethyl acetate (500 mL). Filter the resulting suspension and dry the solid. Add this solid (82.5 g, 338 mmol) in portions to refluxing xylene (1 L), stir for 2 hours, and then cool. Decant the xylene and dissolve the residue in 1N hydrochloric acid (600 mL). Neutralize with sodium carbonate, extract with ethyl acetate (10×500 mL), dry the extracts over sodium sulfate, filter and concentrate under reduced pressure. Subject the residue to silica gel chromatography, eluting with 10-20% diethyl ether in hexanes. Combine fractions containing product and concentrate them under reduced pressure to provide the desired compound (28.1 g, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058425B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-ac299488fc6643b48a92b2795009ca3f |
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| Source note | uspto-grants-2011_11 |
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