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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975495Generated: October 31, 2026

Iodine → 8-(But-3-en-1-yl)-1,4-dioxaspiro[4.5]decan-8-ol

https://huagongshe.com/reaction/1975495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHomoallyl bromideHCID 21241—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
Product8-(But-3-en-1-yl)-1,4-dioxaspiro[4.5]decan-8-olHCID 54241837—

Reaction Steps

To a mixture of 4-bromo-1-butene (1.0 g) and magnesium turnings (1.77 g) in dry tetrahydrofuran (10 mL) was added a crystal of iodine and the mixtures was stirred at room temperature until complete reaction had occurred. To this mixture was added 1,4-cyclohexanedione monoethylene ketal (780 mg) in tetrahydrofuran (1 mL) at 0° C. After 1 h at 0° C. and 1 h at room temperature the reaction mixture was diluted with ammonium chloride solution and the product was extracted with ether. After drying over magnesium sulfate the solvent was removed in vacuo and the residue was subjected to flash chromatography with 25% ethyl acetate /hexane as the eluent to afford 4-(3-Butenyl)-4-hydroxy-cyclohexanone ethylene ketal as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05286860
Source datasetuspto-grants-1994_02
ORD IDord-7009a54330684e7ba6dfb57b9ab1521f
Source noteuspto-grants-1994_02