HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31703Generated: October 29, 2026
Water → 1,4-Dioxaspiro[4.4]nonan-6-ylmethanol
https://huagongshe.com/reaction/31703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 1,4-dioxaspiro[4.4]nonane-6-carboxylate | HCID 10559447 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1,4-Dioxaspiro[4.4]nonan-6-ylmethanol | HCID 10487146 | 72.4% |
Reaction Steps
To a suspension of lithium aluminum hydride (630 mg, 16.6 mmol) in diethyl ether (30 ml), methyl 1,4-dioxaspiro[4.4]nonane-6-carboxylate (3.1 g, 16.6 mmol) obtained by the method of the step (80a) above was added at 0° C. The mixture was stirred at room temperature for 3 hours. Water (0.6 ml), a 5N aqueous sodium hydroxide solution (0.6 ml), and water (1.8 ml) were sequentially added at 0° C. to the mixture and the mixture was filtrated. After water was added to the filtrate and the organic layer was separated. The aqueous layer was extracted three times with ethyl acetate. The resultant extract was dried over sodium sulfate, concentrated under reduced pressure, and purified by silica gel column chromatography (elution solvent: ethyl acetate/heptane=1/4, 1/1) to obtain the title compound (1.9 g, yield 72.4%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07425634B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-ca25e294dd11454b8ae7a8855862d95b |
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| Source note | uspto-grants-2008_09 |
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