HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618664Generated: October 31, 2026
2,4-Dichloro-5,7-difluoro-3-methylquinoline → 3-((4-Chloro-5,7-difluoro-3-methylquinolin-2-yl)methyl)benzonitrile
https://huagongshe.com/reaction/1618664
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Dichloro-5,7-difluoro-3-methylquinoline | HCID 59631040 | — |
| Reactant | HCID 178509756 | HCID 178509756 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-((4-Chloro-5,7-difluoro-3-methylquinolin-2-yl)methyl)benzonitrile | HCID 67285422 | — |
Reaction Steps
A screw cap vial was charged with 2,4-dichloro-5,7-difluoro-3-methylquinoline (500 mg, 2.016 mmol), tetrakis(triphenylphosphine)palladium(0) (233 mg, 0.202 mmol), and THF (5.04 mL). The mixture was sparged with N2, then (3-cyanobenzyl)zinc(II) bromide (0.5M in THF, 4.23 mL, 2.116 mmol) was added and the reaction stirred at 60° C. for 2 h. The reaction was then partitioned between EtOAc and water, and the organic layer washed with brine, dried (MgSO4), and concentrated. The crude material was purified by flash chromatography, eluting with a gradient of 0-15% EtOAc in hexane to give 3-((4-chloro-5,7-difluoro-3-methylquinolin-2-yl)methyl)benzonitrile. Mass Spectrum (ESI) m/e=329.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765940B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-8cf4396bdee742e890061360a16698de |
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| Source note | uspto-grants-2014_07 |
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