HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383768Generated: October 25, 2026
1-Fluoro-2-iodobenzene → 8-(2-Fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol
https://huagongshe.com/reaction/1383768
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Fluoro-2-iodobenzene | HCID 67673 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-one | HCID 567415 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(2-Fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol | HCID 21187639 | 30.1% |
Reaction Steps
To a solution of 2-fluoro-1-Iodobenzene (11.1 g, 50.0 mmol) in 50 mL THF, cooled to −78° C. under argon, was added n-butyllithium (20.0 mL 2.5M in hexane, 50.0 mmol). The solution was stirred 10 min. at −78° C., and a solution of 1,4-cyclohexanedione mono-ethylene ketal (7.81 g, 50.0 mmol) in 50 mL THF was added slowly. The solution was warmed to r.t. and stirred for 60 min., then poured onto saturated sodium bicarbonate and extracted with ethylacetate. The combined organic layers were washed with saturated sodium chloride, dried with magnesium sulfate, and concentrated in vacuo. The crude solid was crystallized from dichloromethane/hexane to give 8-(2-Fluoro-phenyl)-1,4-dioxa-spiro-[4.5]decan-8-ol (3.8 g, 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06255315B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-c118451cc169486e90e3685de2868454 |
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| Source note | uspto-grants-2001_07 |
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