HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228817Generated: October 26, 2026
Hexane → (4,5-Dimethylfuran-2-yl)-(6-methyl-pyridin-2-yl)-methanol
https://huagongshe.com/reaction/228817
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-Bromo-6-methylpyridine | HCID 79205 | — |
| Reactant | 4,5-Dimethyl-2-furaldehyde | HCID 643406 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4,5-Dimethylfuran-2-yl)-(6-methyl-pyridin-2-yl)-methanol | HCID 23078353 | 80% |
Reaction Steps
2-Bromo-6-picoline (1.5 g) was dissolved in tetrahydrofuran (40 ml) under an argon atmosphere to prepare a solution. A 1.6 M hexane solution (5.6 ml) of n-butyllithium was added dropwise to the solution at −78° C., and the mixture was then stirred at −78° C. for 30 min. A solution of 4,5-dimethylfurfural (1 g) in tetrahydrofuran (20 ml) was added dropwise thereto, and the temperature of the mixture was raised to room temperature while stirring. Water was added to the reaction solution to stop the reaction, and the solvent was removed by distillation under the reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using hexane-acetone to give (4,5-dimethylfuran-2-yl)-(6-methyl-pyridin-2-yl)-methanol (1.4 g, yield 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560558B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-184fa0e40e7b4fb6846e0d92c287f54f |
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| Source note | uspto-grants-2009_07 |
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