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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106376Generated: October 31, 2026

Iodine → 8-(3-Fluoro-4-iodophenyl)-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/reaction/1106376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant8-(3-Fluorophenyl)-1,4-dioxaspiro[4.5]decaneHCID 18787926—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantSodium BisulfiteHCID 23665763—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product8-(3-Fluoro-4-iodophenyl)-1,4-dioxaspiro[4.5]decaneHCID 18787924—

Reaction Conditions

Temperature-100 °C

Reaction Steps

121.0 g of 8-(3-fluorophenyl)-1,4-dioxaspiro[4.5]decane and 61.7 g of potassium tert-butoxide in 700 ml of THF were introduced into the apparatus and cooled to -100° C. 335.6 ml of a 15% solution of butyllithium in hexane were then added dropwise with stirring at -100° C., and the mixture was stirred at the same temperature for a further 30 minutes. A solution of 139.6 g of iodine in 300 ml of THF was then added dropwise with stirring at from -90 to -100° C., and the mixture was stirred for a further 30 minutes, allowed to warm to -25° C. and hydrolysed using 500 ml of water. 37% NaHSO3 solution was then added until the mixture became colorless. The organic phase was then separated off, and the aqueous phase was extracted with 2×200 ml of methyl tert-butyl ether. The combined organic extracts were washed once with 200 ml of sodium chloride solution, dried using sodium sulfate, filtered and evaporated to a residue, giving 8-(3-fluoro-4-iodophenyl)-1,4-dioxaspiro[4.5]decane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057006
Source datasetuspto-grants-2000_05
ORD IDord-30dc6c069f144fdeb14f5fffdde64149
Source noteuspto-grants-2000_05