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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369732Generated: October 30, 2026

1,2-Dimethoxyethane → HCID 71236365, compound

https://huagongshe.com/reaction/2369732

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-DichloropyridineHCID 33515—
ReactantDibenzofuran-4-boronic acidHCID 2734328—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductHCID 71236365HCID 7123636582%

Reaction Steps

Dibenzo[b,d]furan-4-ylboronic acid (25 g, 118 mmol), 2,4-dichloropyridine (19.2 g, 130 mmol), Pd(PPh3)4 (4.1 g, 3.5 mmol) and potassium carbonate (48.9 g, 354 mmol) were added to dimethoxyethane (200 mL) and water (200 mL). The reaction mixture was degassed with nitrogen before being heated to reflux overnight. EtOAc and water were added, the organic layer separated and the aqueous layer was extracted with 3×50 mL dichloromethane and dried over sodium sulfate. After removing the solvent under reduced pressure, the crude product was chromatographed on silica gel with dichloromethane to yield 33.4 g of crude product. The product was crystallized from hexane to give 27.0 g (82%) of 4-chloro-2-(dibenzo[b,d]furan-4-yl)pyridine as white needles. The product was confirmed by GC/MS and NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08709615B2
Source datasetuspto-grants-2014_04
ORD IDord-4c37b04c6abf4a0fad48c47422a9128a
Source noteuspto-grants-2014_04