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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578817Generated: November 3, 2026

Sodium Carbonate → 5-(Bromomethyl)-3-(3-(difluoromethoxy)phenyl)-2-ethoxypyrazine

https://huagongshe.com/reaction/578817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBoronic AcidHCID 61668—
Reactant3-Bromo-2-ethoxy-5-methylpyrazineHCID 90414639—
Reactant3-(3-(Difluoromethoxy)phenyl)-2-ethoxy-5-methylpyrazineHCID 90415580—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product5-(Bromomethyl)-3-(3-(difluoromethoxy)phenyl)-2-ethoxypyrazineHCID 9041481690%

Reaction Steps

3-(3-(Difluoromethoxy)phenyl)-2-ethoxy-5-methylpyrazine. A solution of 3-bromo-2-ethoxy-5-methylpyrazine (1.80 g, 8.29 mmol), 3-(difluoromethoxy)phenyl)boronic acid (2.03 g, 10.78 mmol), tetrakis(triphenylphosphine) palladium(0) (958.25 mg, 0.83 mmol), sodium carbonate (21.63 mL, 1.15 mol/L, 24.88 mmol), in EtOH (22 mL) and toluene (118 mL), under nitrogen, was heated at 88° C. for 1 h. The reaction mixture was extracted with EtOAc. The combined organic layers were dried (Na2SO4), and the solvent was removed under reduced pressure. Purification (FCC, SiO2, 0-50%, EtOAc/hexanes) afforded the title compound as a colorless oil (2.09 g, 90%). [M+H]=281.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040692B2
Source datasetuspto-grants-2015_05
ORD IDord-0d9a870838244ce48fa6a7b22f458837
Source noteuspto-grants-2015_05