HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192655Generated: November 2, 2026
HCID 59226455, compound → HCID 59226612, compound
https://huagongshe.com/reaction/2192655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59226455 | HCID 59226455 | — |
| Reactant | HCID 178477796 | HCID 178477796 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59226612 | HCID 59226612 | — |
Reaction Steps
To a solution of methyl 6-(2,6-difluoro-3-(trifluoromethylsulfonyloxy)-phenyl)picolinate (1.0 equiv.) in toluene was added Pd(dppf)Cl2-DCM (0.1 equiv.) followed by dimethyl zinc (3.0 equiv.). The solution turned from orange to bright yellow. The reaction was heated to 80° C. for 2 hours at which time, LC/MS analysis indicated complete conversion to product. The reaction was cooled to room temperature, diluted with ethyl acetate and washed with brine. The organic layer was dried with magnesium sulfate, filtered, and concentrated in vacuo to provide methyl 6-(2,6-difluoro-3-methylphenyl)picolinate as a brown oil in quantitative yield. LC/MS=264.0 (M+H), Rt=0.90 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329732B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-c260d80db12248a1ada70803a04dcff0 |
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| Source note | uspto-grants-2012_12 |
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