HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610702Generated: October 31, 2026
Water → 2-methyl-2-(3-methylphenyl)propan-1-ol
https://huagongshe.com/reaction/1610702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl α,α,3-trimethylbenzeneacetate | HCID 22261616 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-methyl-2-(3-methylphenyl)propan-1-ol | HCID 316758 | — |
Reaction Steps
To a suspension of lithium aluminum hydride (3.52 g, 92.9 mmol) in tetrahydrofuran (150 ml) was dropwise added a solution of ethyl 2-methyl-2-(3-methylphenyl)propionate (19.16 g, 92.88 mmol) in tetrahydrofuran (100 ml) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. After ice-cooling the reaction solution, water (3.5 ml), 15% aqueous sodium hydroxide solution (3.5 ml) and water (9 ml) were successively added dropwise to decompose excess lithium aluminum hydride. The mixture was stirred as it was at room temperature for 2 hrs. The resulting precipitate was removed by filtration, and the precipitate was washed with ethyl acetate. The solvent of the recovered filtrate was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=6/1) to give the objective substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06982348B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-49efef22fe364fc8a56a5aac02db39de |
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| Source note | uspto-grants-2006_01 |
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