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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578825Generated: November 3, 2026

Sodium Carbonate → 5-(Bromomethyl)-2-(difluoromethoxy)-3-(3-(oxetan-3-yloxy)phenyl)pyridine

https://huagongshe.com/reaction/578825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(3-hydroxyphenyl)boronic AcidHCID 2734359—
Reactant3-Bromo-5-(bromomethyl)-2-(difluoromethoxy)pyridineHCID 90414793—
Reactant3-(2-(Difluoromethoxy)-5-methylpyridin-3-yl)phenolHCID 90415202—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product5-(Bromomethyl)-2-(difluoromethoxy)-3-(3-(oxetan-3-yloxy)phenyl)pyridineHCID 9041497291%

Reaction Conditions

Temperature100 °C

Reaction Steps

3-(2-(Difluoromethoxy)-5-methylpyridin-3-yl)phenol. A 20 mL microwave vial was charged with 3-bromo-2-(difluoromethoxy)-5-methylpyridine (intermediate 4, 1.90 g, 7.98 mmol), 3-hydroxyphenylboronic acid (1.32 g, 9.58 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (330 mg, 0.40 mmol), sodium carbonate (2.12 g, 19.96 mmol), water (4.0 mL), and ACN (12 mL). The vial was sealed, purged with nitrogen, and heated under microwave irradiation at 100° C. for 15 min. The reaction mixture was diluted with water and extracted with DCM (3×). The combined organic phase was dried (Na2SO4), filtered, and concentrated under reduced pressure. Purification (FCC, SiO2, 0-40% EtOAc/hexanes) afforded the title compound (1.81 g, 91%) as a colorless waxy solid. [M+H]=252.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040692B2
Source datasetuspto-grants-2015_05
ORD IDord-3f0f4f4bcfb148058c43b0e669d8608f
Source noteuspto-grants-2015_05