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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | 8-(3-Fluorophenyl)-1,4-dioxaspiro[4.5]decane | HCID 18787926 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 8-(3-Fluoro-4-iodophenyl)-1,4-dioxaspiro[4.5]decane | HCID 18787924 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057006 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-30dc6c069f144fdeb14f5fffdde64149 |
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| Source note | uspto-grants-2000_05 |
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