HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610342Generated: October 30, 2026
Water → (2,2-Difluoro-1,3-dioxaindan-5-yl)methanol
https://huagongshe.com/reaction/1610342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,2-Difluoro-1,3-benzodioxole-5-carboxylic acid | HCID 608772 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2,2-Difluoro-1,3-dioxaindan-5-yl)methanol | HCID 12814281 | — |
Reaction Steps
To a suspension of lithium aluminum hydride (1.86 g, 48.9 mmol) in tetrahydrofuran (30 ml) was dropwise added a solution of 2,2-difluoro-1,3-benzodioxole-5-carboxylic acid (4.942 g, 24.45 mmol) in tetrahydrofuran (30 ml) under ice-cooling and the mixture was stirred at room temperature for 1 hr. The reaction solution was ice-cooled and water (2 ml), 15% aqueous sodium hydroxide solution (2 ml) and water (5 ml) was dropwise added successively 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 collected filtrate was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=6/1−1/1) 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-30a1d55276474b3195226883b61eedbb |
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| Source note | uspto-grants-2006_01 |
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