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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095686Generated: October 30, 2026

Sodium Bicarbonate → 4-bromo-3-methoxy-1-methyl-1H-pyrazole

https://huagongshe.com/reaction/2095686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3-Methoxy-1-methyl-1H-pyrazoleHCID 18622370—
ReactantPyridiniumtribromideHCID 21124087—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-bromo-3-methoxy-1-methyl-1H-pyrazoleHCID 67003909—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-methoxy-1-methyl-1H-pyrazole (0.500 g, 4.46 mmol) in MeOH (50.0 mL) was cooled to 0° C. and charged with pyridinium tribromide (1.43 g, 4.46 mmol) in portions. The solution was stirred for 1 h at 0° C. then for an additional 16 h at rt. The reaction mixture was charged with sat. NaHCO3 (2.5 mL) and diluted with H2O and extracted with CHCl3 (3×). The combined organic fractions were dried over Na2SO4, filtered and concentrated in vacuo resulting in the title compound as a red oil. This material was used in the next step without further purification. 1H NMR (400 MHz, CD3OD): δ=3.66 (s, 3H), 4.07 (s, 3H), 7.30 (s, 1H). MS (ES+): m/z 190.98, 192.99 (49.5/50.5) [MH+]. HPLC: tR=2.29 min (polar—5 min, ZQ3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445510B2
Source datasetuspto-grants-2013_05
ORD IDord-dad150b2e7b147419b31436ff62ae93c
Source noteuspto-grants-2013_05