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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845372Generated: October 30, 2026

Potassium Carbonate → 5-(1-methyl-1H-pyrazol-5-yl)thiophene-2-carboxylic acid

https://huagongshe.com/reaction/1845372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromothiophene-2-carboxylic acidHCID 349115—
Reactant5-(5,5-Dimethyl-1,3,2-dioxaborinan-2-YL)-1-methyl-1H-pyrazoleHCID 44119444—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product5-(1-methyl-1H-pyrazol-5-yl)thiophene-2-carboxylic acidHCID 58657329—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 5-bromo-2-thiophenecarboxylic acid (100 mg, 0.48 mmol) in dioxane/H2O (5:1, 6 mL) was added K2CO3 (267 mg, 1.93 mmol), tetrakistriphenylphosphine Pd(0) (28 mg, 24 umol) and 5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1-methyl-1H-pyrazole (94 mg, 0.48 mmol). The reaction mixture was heated to 80° C. in a sealed tube for 12 h and was then partitioned between 6N NaOH and DCM. The pH of the aqueous phase was adjusted to ˜3 with 3M HCl and washed several times with DCM. The combined organic fractions were dried (Na2SO4), concentrated under vacuum and used directly without further purification (−100 mg, quant.): LC-MS (ES) m/z=209 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946278B2
Source datasetuspto-grants-2015_02
ORD IDord-ae5548fc422540feb3f43e0aebfd901c
Source noteuspto-grants-2015_02