HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200570Generated: October 29, 2026
Ethyl Acetate → 2-(2-Ethyl-1,3-dioxolan-2-yl)ethan-1-ol
https://huagongshe.com/reaction/2200570
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methyl (2-ethyl-1,3-dioxolan-2-yl)acetate | HCID 13085711 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Ethyl-1,3-dioxolan-2-yl)ethan-1-ol | HCID 13940368 | 27.7% |
Reaction Steps
To a solution of methyl 2-(2-ethyl-1,3-dioxolan-2-yl)acetate (1 g, 5.75 mmol) in anhydrous THF (40 mL) was added LAH (900 mg, 23.7 mmol) at 0° C. under nitrogen atmosphere, the resulting mixture was stirred at 90° C. overnight. The mixture was cooled to room temperature, and ethyl acetate was added to the mixture. The resulting slurry was filtered and the filtrate was concentrated to dryness. The crude product was purified by silica gel chromatography eluting with DCM/methanol (100:1 to 20:1) to give 2-(2-ethyl-1,3-dioxolan-2-yl)ethanol (233 mg, 27.4%) as yellow oil that was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359359B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-a3ea0c00eed240358c5ab40bec1d22c9 |
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| Source note | uspto-grants-2016_06 |
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