HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369733Generated: October 29, 2026
1,2-Dimethoxyethane → HCID 71007915, compound
https://huagongshe.com/reaction/2369733
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Dibenzofuran-4-boronic acid | HCID 2734328 | — |
| Reactant | 2,5-Dibromo-4-methylpyridine | HCID 2734429 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 71007915 | HCID 71007915 | 72.2% |
Reaction Steps
2,5-Dibromo-4-methylpyridine (30 g, 118 mmol), dibenzo[b,d]furan-4-ylboronic acid (25 g, 118 mmol), Pd(PPh3)4 (1.4 g, 1.18 mmol), and K2CO3 (49 g, 354 mmol) were added to a flask with dimethoxyethane (450 mL) and water (100 mL) and degassed with nitrogen. The reaction mixture was heated to reflux for 15 h before cooling to room temperature. 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 and 29.7 g of crude product was obtained. The product was crystallized from hexane to give 28.8 g (72%) of pure product. The product was confirmed by NMR and HPLC (99.3% pure)
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-d1aac974cdce4a36afc85d0ef1e1d73f |
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| Source note | uspto-grants-2014_04 |
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