HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456050Generated: October 27, 2026
Sodium Formate → 7-Fluoroquinoline-6-carbaldehyde
https://huagongshe.com/reaction/456050
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | 6-Bromo-7-fluoroquinoline | HCID 14548343 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Fluoroquinoline-6-carbaldehyde | HCID 52982909 | 10.4% |
Reaction Steps
To a suspension of Pd(PPh3)4 (1.27 g, 1.1 mmol) and sodium formate (13.8 g, 132 mmol, 6 e.q.) in acetonitrile (30 mL) was added a solution of 6-bromo-7-fluoro quinoline (5 g, 22 mmol) in DMSO (30 mL). The reaction mixture was heated at 120° C. under a CO atmosphere (1 MPa) for 4 h, cooled to rt and concentrated under reduced pressure. The residue was partitioned between water (100 mL) and ethyl acetate (150 mL). The organic layer was separated, washed with brine (100 mL), dried over Na2SO4 and concentrated under reduced pressure. The reside was purified by column choromatography, eluting with petroleum:ethyl acetate=10:1˜3:1 to give the title compound as a white solid (400 mg, 10.4%). 1H-NMR (400 MHz, DMSO-d6) δ ppm 8.95 (s, 1H), 8.46 (m, 1H), 8.20 (m, 1H), 7.75 (d, 1H), 7.53 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497368B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-899d9ddf6da3423f866f6eb2b983a8b3 |
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| Source note | uspto-grants-2013_07 |
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