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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961027Generated: October 29, 2026

Potassium Carbonate → HCID 57826760, compound

https://huagongshe.com/reaction/1961027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-bromo-4-methylthiophene-2-carboxylateHCID 2795489—
Reactant5-(5,5-Dimethyl-1,3,2-dioxaborinan-2-YL)-1-methyl-1H-pyrazoleHCID 44119444—
CatalystHCID 178418397HCID 178418397—
CatalystHCID 178418851HCID 178418851—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 57826760HCID 57826760—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 5-bromo-4-methyl-2-thiophenecarboxylate (1 g, 4.25 mmol) in dioxane/H2O (5:1, 20 mL) was added K2CO3 (2.3 g, 17 mmol), bis(tri-t-butylphosphine)palladium(0) (108 mg, 0.213 mmol) and 5-(5,5-dimethyl-1,3,2-dioxaborinane-2-yl)-1-methyl-1H-pyrazole (1.2 g, 5.52 mmol). The reaction mixture was heated to 80° C. in a sealed tube for 2 h and additional tetrakistriphenylphosphine Pd(0) (279 mg, 0.241 mmol) and 5-(5,5-dimethyl-1,3,2-dioxaborinane-2-yl)-1-methyl-1H-pyrazole (1.2 g, 6.27 mmol) were added. After 12 h, the reaction was partitioned between H2O-DCM and the aqueous phase was washed several times with DCM. The combined organic fractions were dried over Na2SO4, concentrated and used directly without further purification: LCMS (ES) m/z=237 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410158B2
Source datasetuspto-grants-2013_04
ORD IDord-bd325efdec23488486691a93c7c47239
Source noteuspto-grants-2013_04