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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369730Generated: October 30, 2026

1,2-Dimethoxyethane → HCID 71236373, compound

https://huagongshe.com/reaction/2369730

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
Reactant2,5-DichloropyridineHCID 27685—
ReactantDibenzofuran-4-boronic acidHCID 2734328—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductHCID 71236373HCID 7123637376%

Reaction Steps

Dibenzo[b,d]furan-4-ylboronic acid (9.5 g, 44.8 mmol), 2,5-dichloropyridine (7.0 g, 47.0 mmol), Pd(PPh3)4 (2.6 g, 2.2 mmol) and potassium carbonate (18.6 g, 134 mmol) were added to dimethoxyethane (75 mL) and water (75 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 11.7 g of crude product. The product was crystallized from hexane to give 9.5 g (76%) of 5-chloro-2-(dibenzo[b,d]furan-4-yl)pyridine as white needles. The product was confirmed by GC/MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08709615B2
Source datasetuspto-grants-2014_04
ORD IDord-5a6e59021f62482588d57eca910e9c2d
Source noteuspto-grants-2014_04