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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908765Generated: October 27, 2026

Potassium Carbonate → HCID 67026909, compound

https://huagongshe.com/reaction/1908765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant2,4,6-Trivinylboroxin-Pyridine ComplexHCID 2734806—
ReactantHCID 10933837HCID 10933837—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67026909HCID 6702690983.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5,6-dichloronicotinic acid tert.-butyl ester (5.00 g, 20.0 mmol), and 2,4,6-trivinylcyclotriboroxane pyridine complex (9.700 mg, 40 mmol) in dioxane (30 mL), a solution of 2 M aq. K2CO3 (6 mL) followed by Pd(PPh3)4 (620 mg, 0.38 mmol) and triphenylphosphine (620 mg, 3.8 mmol) is added. The mixture is stirred at 100° C. for 2 h, cooled to rt and diluted with diethyl ether (200 mL). The mixture is extracted with 1M aq. NaOH (2×50 mL) and brine (50 mL). The org. phase is dried (Na2SO4), filtered and evaporated. The residue is purified by FC (SiO2, EA-heptane) to give 5-chloro-6-vinyl-nicotinic acid tert.-butyl ester (4.0 g) as a yellow oil; LC-MS: tR=1.05 min, [M+1+CH3CN]+=281.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598208B2
Source datasetuspto-grants-2013_12
ORD IDord-d4a00a91f42d4c75a70325967a08a2b5
Source noteuspto-grants-2013_12