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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,6-Difluorophenylboronic acidHCID 2734336—
Reactant6-Bromo-3-fluoro-2-methylpyridineHCID 2783180—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product6-(2,6-Difluorophenyl)-3-fluoro-2-methylpyridineHCID 5922652788%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592455B2
Source datasetuspto-grants-2013_11
ORD IDord-af46105fa280425e8bb7ab4e5d873850
Source noteuspto-grants-2013_11