HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888286Generated: October 31, 2026
Lithium borohydride → (8-(Benzyloxymethyl)-1,4-dioxaspiro[4.5]decan-8-yl)methanol
https://huagongshe.com/reaction/888286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Ethyl 8-(benzyloxymethyl)-1,4-dioxaspiro[4.5]decane-8-carboxylate | HCID 58399380 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (8-(Benzyloxymethyl)-1,4-dioxaspiro[4.5]decan-8-yl)methanol | HCID 58399365 | 75% |
Reaction Steps
To a solution of ethyl 8-(benzyloxymethyl)-1,4-dioxaspiro[4.5]decane-8-carboxylate (Reference Example 84) (279 mg, 0.834 mmol) in tetrahydrofuran (4.2 mL), lithium borohydride (91.0 mg, 4.17 mmol) was added with stirring under ice-cooling, and the obtained solution was stirred at 70° C. for 4 hours. The reaction was quenched by adding saturated aqueous ammonium chloride solution to the reaction solution, and the resulting solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, n-hexane/ethyl acetate) to obtain the captioned compound (183 mg, 0.625 mmol, 75%) as a colorless oily compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247569B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-9f3ed6d0ea6c4ae8864f655fd4b38eb6 |
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| Source note | uspto-grants-2012_08 |
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