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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752039Generated: October 27, 2026

Water → tetrahydro-4-(4-iodophenyl)-2H-pyran-4-ol

https://huagongshe.com/reaction/1752039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-DiiodobenzeneHCID 12208—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Producttetrahydro-4-(4-iodophenyl)-2H-pyran-4-olHCID 57033480—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under an argon atmosphere, a solution of n-butyllithium (2.59M, in hexane) (8.76 ml) was added dropwise to a solution of 1,4-diiodobenzene (7.49 g) in anhydrous THF (50 ml) at −78° C., and the resulting mixture was stirred at −78° C. for minutes. Tetrahydro-4H-pyran-4-one (2.09 ml) was added dropwise thereto and the resulting mixture was stirred at −78° C. for 1.5 hours. After stirring the mixture for another 3 hours at room temperature, water was added, and the resulting mixture was extracted with ethyl acetate. Organic layer was washed once with water and once with saturated brine, and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was recrystallized from cyclohexane/ethyl acetate mixed solvent to obtain tetrahydro-4-(4-iodophenyl)-2H-pyran-4-ol (4.12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162988B2
Source datasetuspto-grants-2015_10
ORD IDord-860e97d382de413fb33650c9eda0af1a
Source noteuspto-grants-2015_10