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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641103Generated: November 2, 2026

Dimethylformamide → 8-Vinyl-1,4-dioxaspiro[4,5]decane

https://huagongshe.com/reaction/641103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHeptaneHCID 8900—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant8-(2-Iodoethyl)-1,4-dioxaspiro[4.5]decaneHCID 57598630—
SolventWaterHCID 962—
Product8-Vinyl-1,4-dioxaspiro[4,5]decaneHCID 5759891978%

Reaction Conditions

Temperature3 °C

Reaction Steps

233.0 g of the compound (21) and 800 mL of DMF were added to a reactor under nitrogen atmosphere, and stirred at 3° C. under cooling with ice. 92.9 g of potassium t-butoxide (t-BuOK) was added thereto by dividing into 10 portions at a temperature range of from 3 to 10° C. over 2 hours, followed by further stirring at 0° C. for 3 hours. After confirming that the reaction had been completed by GC analysis, the reaction mixture was poured into and mixed with a mixture of 1,500 mL of heptane and 1,500 mL of water at 0° C. The mixture was separated into an organic layer and an aqueous layer by standing still, so as to attain extraction to the organic layer. The resulting organic layer was fractionated and washed with water, followed by drying over anhydrous magnesium sulfate. The resulting organic layer was purified by silica gel column chromatography using heptane as eluent, and the solvent was removed by distillation under reduced pressure. The resulting residue was distilled under reduced pressure to obtain 103.3 g of 8-vinyl-1,4-dioxaspiro[4,5]decane (22) as a colorless transparent liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07695777B2
Source datasetuspto-grants-2010_04
ORD IDord-69fd013b738e4342b40e8a3fd3a1a083
Source noteuspto-grants-2010_04