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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235971Generated: October 30, 2026

Potassium Carbonate → 6-Chloro-2,3-dimethylpyridine

https://huagongshe.com/reaction/2235971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant5,6-Dimethyl-2-pyridoneHCID 119785—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product6-Chloro-2,3-dimethylpyridineHCID 1250837677.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

5,6-dimethyl-2(1H)pyridinone (Example 476, 0.39 g, 3.2 mmol) was suspended in phosphorous oxychloride (5.00 mL, 53.6 mmol) and heated to 100° C. Then, phosphorous pentachloride (4.00 g, 19.2 mmol) was added, and the mixture was heated to 140° C. After 16 h, the mixture was cooled to rt, diluted with CH2Cl2 (5 mL), and slowly poured into a 0° C. solution of potassium hydroxide (5 g) and potassium carbonate (5 g) in water (100 mL). Upon complete addition, the mixture was allowed to warm to rt and stirred for 1 h. The aqueous solution was extracted with CH2Cl2, and the combined organics layers were dried (MgSO4), filtered, and concentrated in vacuo to provide the title compound (0.35 g, 77%) as a brown oil. The material was used in the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 7.36 (d, 1H), 7.07 (d, 1H), 2.49 (s, 3H), 2.27 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714004B2
Source datasetuspto-grants-2010_05
ORD IDord-1dd36045d76f4e8baa8741b221a80be5
Source noteuspto-grants-2010_05