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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802528Generated: November 1, 2026

Lithium borohydride → (8-(Benzyloxymethyl)-1,4-dioxaspiro[4.5]decan-8-yl)methanol

https://huagongshe.com/reaction/1802528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantEthyl 8-(benzyloxymethyl)-1,4-dioxaspiro[4.5]decane-8-carboxylateHCID 58399380—
SolventTetrahydrofuranHCID 8028—
Product(8-(Benzyloxymethyl)-1,4-dioxaspiro[4.5]decan-8-yl)methanolHCID 5839936575%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349874B2
Source datasetuspto-grants-2013_01
ORD IDord-738a9960a5cc414b832831943a8c490e
Source noteuspto-grants-2013_01