HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046870Generated: November 2, 2026
Diisopropylethylamine → 6-(2,6-Difluorophenyl)-3-fluoro-2-methylpyridine
https://huagongshe.com/reaction/2046870
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,6-Difluorophenylboronic acid | HCID 2734336 | — |
| Reactant | 6-Bromo-3-fluoro-2-methylpyridine | HCID 2783180 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-(2,6-Difluorophenyl)-3-fluoro-2-methylpyridine | HCID 59226527 | 88% |
Reaction Steps
To a solution of 6-bromo-3-fluoro-2-methylpyridine (1.0 equiv.) in ethanol and toluene (1:1, 0.2 M) was added 2,6-difluorophenylboronic acid, DIEA (5 equiv.) and Pd(PPh3)4 (0.2 equiv.). The reaction was heated in the microwave at 120° C. for 30 min. The solution was filtered and rinsed with ethyl acetate. The volatiles were removed in vacuo and the crude was purified via silica gel column chromatography eluting with ethyl acetate and hexanes (2.5-20% ethyl acetate). Upon concentration of the pure fractions, 6-(2,6-difluorophenyl)-3-fluoro-2-methylpyridine was isolated in 88% yield. LC/MS=224.1 (M+H), Rt=0.87 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592455B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-af46105fa280425e8bb7ab4e5d873850 |
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| Source note | uspto-grants-2013_11 |
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