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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748506Generated: November 1, 2026

Water → 1,4-Dioxaspiro[4.5]decane-8-carbonitrile

https://huagongshe.com/reaction/1748506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1,4-Dioxaspiro[4.5]decane-8-carbonitrileHCID 1111643372%

Reaction Steps

p-Toluenesulfonylmethylisocyanide (27.0 g) was added at room temperature to a solution of 1,4-cyclohexanedione monoethyleneketal (16.6 g) in 1,2-dimethoxyethane (133 ml) and ethanol (13 ml). Then, potassium tert-butoxide was added under ice cooling over an hour, and stirred at room temperature for three hours. After completion of the reaction, water was added and extracted with ethyl acetate three times. The organic layer was dried over anhydrous sodium sulfate and concentrated. The resulting residue was purified with silica gel column chromatography (n-hexane/ethyl acetate) to give 1,4-dioxaspiro[4,5]decane-8-carbonitrile (12.8 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-41cda5b126f94b108dbf6a875ef39b3d
Source noteuspto-grants-2015_10