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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452018Generated: October 28, 2026

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

https://huagongshe.com/reaction/1452018

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 actetate/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 numberUS05606059
Source datasetuspto-grants-1997_02
ORD IDord-af193dc80df5459689b68667c62a8d8b
Source noteuspto-grants-1997_02