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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927342Generated: October 25, 2026

Potassium Carbonate → 6-Cyclohexenyl-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/927342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromopyridine-2-carboxylic acidHCID 593919—
Reactant1-Cyclohexenylboronic acidHCID 3862902—
CatalystHCID 178418807HCID 178418807—
SolventWaterHCID 962—
Product6-Cyclohexenyl-pyridine-2-carboxylic acidHCID 7108723361.2%

Reaction Steps

Under an atmosphere of nitrogen, a solution of 6-bromo-pyridine-2-carboxylic acid (CAN 1190-87-4, 3 g, 6.4 mol), cyclohexenylboronic acid (CAN 21190-87-4, 0.89 g, 7.1 mmol), 1,1′-bis(diphenyl-phosphino)ferrocene-palladium(II)dichloride methylene chloride complex (CAN 95464-05-4, 8 mg, 0.13 mmol), potassium carbonate (1.78 g, 12.9 mmol) in H2O (30 mL) was heated to 100° C. overnight. The reaction mixture was extracted with ethyl acetate (50 mL). The pH of the aqueous layer was adjusted to 5 by addition of 1 N hydrochloric acid and the resulting mixture was extracted with ethyl acetate (3×50 mL). The combined organic extracts were washed with water and brine, dried over anhydrous sodium sulfate and evaporated. The residue was purified by prep-HPLC to yield the title compound (0.8 g, 3.94 mmol, 61.2%) as yellow oil; MS (EI): m/e=204.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290451B2
Source datasetuspto-grants-2016_03
ORD IDord-7985a38b8bfa4040a747141ca1ca774c
Source noteuspto-grants-2016_03