HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061476Generated: November 2, 2026
Ethylene Oxide → 2-(5-Methylfuran-2-yl)ethan-1-ol
https://huagongshe.com/reaction/1061476
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | 2-Methylfuran | HCID 10797 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(5-Methylfuran-2-yl)ethan-1-ol | HCID 11062390 | 72.5% |
Reaction Steps
A solution of n-BuLi (83 mL, 133.0 mmol, 1.2 eq, 1.6 M in hexanes) was added to a stirred solution of 2-methylfuran (10 mL, 110.8 mmol, 1 eq) in THF (85 mL) at 0° C. under inert atmosphere. The reaction mixture was stirred for 4 h at room temperature then cooled to 0° C. Ethylene oxide (8.3 mL, 166.3 mmol, 1.5 eq) was added dropwise and the reaction mixture was allowed to warm to room temperature overnight. After quenching with saturated aqueous NH4Cl, the resulting layers were separated and the aqueous layer was extracted with Et2O (2×). The combined organic layers were dried over Na2SO4 and concentrated under reduced pressure. Distillation at atmospheric pressure (170-185° C.) gave 10.13 g (80.3 mmol, 72%) of 5-methyl-2-furanethanol (2f(2)) as a light yellow oil:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06960474B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-c67773a842d44d21a64959c4b7aa354a |
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| Source note | uspto-grants-2005_11 |
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