HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369730Generated: October 30, 2026
1,2-Dimethoxyethane → HCID 71236373, compound
https://huagongshe.com/reaction/2369730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Dichloropyridine | HCID 27685 | — |
| Reactant | Dibenzofuran-4-boronic acid | HCID 2734328 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 71236373 | HCID 71236373 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08709615B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-5a6e59021f62482588d57eca910e9c2d |
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| Source note | uspto-grants-2014_04 |
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