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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-2-iodobenzeneHCID 67673—
ReactantSodium BicarbonateHCID 516892—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product8-(2-Fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-olHCID 2118763930.1%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255315B1
Source datasetuspto-grants-2001_07
ORD IDord-c118451cc169486e90e3685de2868454
Source noteuspto-grants-2001_07