Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631306Generated: November 1, 2026

Water → 3-BroMo-5-fluoro-2-Methyl-pyridine

https://huagongshe.com/reaction/1631306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantMethylboronic AcidHCID 139377—
Reactant2,3-Dibromo-5-fluoropyridineHCID 22832093—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product3-BroMo-5-fluoro-2-Methyl-pyridineHCID 6684787232.2%

Reaction Conditions

Temperature110 °C

Reaction Steps

2,3-Dibromo-5-fluoropyridine (5.0 g, 19.6 mmol), Pd(PPh3)4 (1.13 g, 0.98 mmol) and methyl boronic acid (3.52 g, 58.9 mmol) were combined in dioxane (50 mL) then treated with K2CO3 (8.13, 58.9 mmol) and water (10 mL). The mixture was purged with N2 then heated to 110° C. in a sealed vessel for 16 hours. The cooled mixture was partitioned between water (100 mL) and EtOAc (50 mL) and the layers separated. The aqueous layer was extracted with EtOAc (2×50 mL) and the combined organic phases were washed with brine (50 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel column chromatography eluting with 1-3% EtOAc/hexanes to afford the product as a white solid (1.20 g, 32% yield). MS (apci) m/z=190.2 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791123B2
Source datasetuspto-grants-2014_07
ORD IDord-bf065f4376e44ae3b8dc28b978f251c0
Source noteuspto-grants-2014_07