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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243765Generated: October 29, 2026

Potassium Carbonate → 3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-fluoro-4,5-dimethylpyridine

https://huagongshe.com/reaction/243765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTrimethylboroxineHCID 574072—
Reactant3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-fluoro-4-iodo-5-methylpyridineHCID 23082581—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product3-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-fluoro-4,5-dimethylpyridineHCID 2308258570.3%

Reaction Steps

1.50 g (3.37 mmol) of 3-(2,3,4-trimethoxy-6-methylbenzoyl)-2-fluoro-4-iodo-5-methylpyridine obtained in Step (c), 1.40 g (10.1 mmol) of potassium carbonate, 0.39 g (0.34 mmol) of tetrakis(triphenylphosphine)palladium, 15 ml of dioxane and 0.42 g (1.67 mmol) of 50% trimethylboroxin were mixed, followed by reflux with heating for 6 hours. After cooling to room temperature, filtration on the pad of celite and washing with ethyl acetate and tetrahydrofuran were carried out, the solvent was distilled off under reduced pressure, and the obtained crude product was purified by silica gel chromatography to obtain 0.79 g (yield: 70%) of 3-(2,3,4-trimethoxy-6-methylbenzoyl)-2-fluoro-4,5-dimethylpyridine (Compound No. 19).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653277B2
Source datasetuspto-grants-2014_02
ORD IDord-bfda7531ef0c4a7e801ce26b30b13a37
Source noteuspto-grants-2014_02