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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089168Generated: November 2, 2026

Ethyl 1,4-dioxaspiro(4.5)decane-8-carboxylate → 1,4-Dioxaspiro[4.5]decan-8-ylmethanol

https://huagongshe.com/reaction/2089168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1,4-dioxaspiro(4.5)decane-8-carboxylateHCID 10488810—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product1,4-Dioxaspiro[4.5]decan-8-ylmethanolHCID 10080838—

Reaction Steps

To 1,4-dioxa-spiro[4.5]decane-8-carboxylic acid ethyl ester (5.7 g, 26.6 mmol) in THF (15 mL) at 0° C. was treated with LAH (1N in THF, 32 mL, 32 mmol) dropwise for 30 min. The reaction was then slowly warmed to room temperature and quenched with MeOH (˜0.5 mL) and filtered through a pad of Celite to give (1,4-dioxa-spiro[4.5]dec-8-yl)-methanol, which was then treated with 1N HCl (5 mL) in acetone (10 mL) at room temperature for 2 hours. The solvent was removed and the solution was then partitioned between ethyl acetate and saturated NaHCO3. The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated to give the crude material, which was purified by silica gel column (hexanes:ethyl acetate 4:1) to afford the title compound as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436023B2
Source datasetuspto-grants-2013_05
ORD IDord-2f9d3dd8c2a34ffd91b83527f49ae051
Source noteuspto-grants-2013_05