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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570185Generated: October 25, 2026

Potassium Carbonate → 4-bromo-5-tert-butyl-2-methyl-2H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/570185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromineHCID 24408—
Reactantethyl 3-(tert-butyl)-1-methyl-1H-pyrazole-5-carboxylateHCID 2799344—
SolventDichloromethaneHCID 6344—
Product4-bromo-5-tert-butyl-2-methyl-2H-pyrazole-3-carboxylic acid ethyl esterHCID 14793344—

Reaction Steps

To a mixture of 5-tert-butyl-2-methyl-pyrazole-3-carboxylic acid ethyl ester (2.00 g, 9.51 mmol) and K2CO3 (3.94 g, 28.5 mmol) in DCM (120 mL), in the dark, was added Br2 (1.46 mL, 28.5 mmol) slowly under Ar. After stirring at room temperature for 3 h under Ar, the resulting mixture was quenched with saturated aqueous Na2S2O3 (50 mL). The organic layer was separated and washed with H2O (50 mL) and brine (50 mL), then dried with Na2SO4. Removal of the solvent under reduced pressure yielded a white solid. 1H-NMR (400 MHz, CDCl3) δ: 4.40 (q, J=7.1 Hz, 2H), 4.08 (s, 3H), 1.43 (t, J=7.1 Hz, 3H), 1.42 (m, 9H). Mass Spectrum (LCMS, ESI pos.) Calculated For C11H17BrN2O2: 289.1 (M+H), Measured: 289.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023846B2
Source datasetuspto-grants-2015_05
ORD IDord-6068e5464a65454e84925cd59103ee60
Source noteuspto-grants-2015_05