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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368756Generated: November 1, 2026

Iodine → 2-(4-Fluorophenyl)bicyclo[2.2.1]heptan-2-ol

https://huagongshe.com/reaction/2368756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantBicyclo(2.2.1)heptan-2-oneHCID 10345—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Fluorophenyl)bicyclo[2.2.1]heptan-2-olHCID 22297833—

Reaction Steps

A mixture of 1-bromo-4-fluorobenzene (5.00 ml, 45.5 mmol), magnesium turnings (3.32 g, 137 mmol), and a few iodine crystals in 70 ml dry THF were vigorously stirred for 4 hours under the protection of nitrogen and cooling with ice/water. Norcamphor (5.00 g, 45.5 mmol) dissolved in 10 ml dry THF was added drop-wise, and the reaction was allowed to warm up to room temperature and stirred overnight. The reaction was carefully quenched with water and decanted from the excess magnesium turnings. The reaction mixture in THF and water was adjusted to pH 7 with 2N HCl solution and extracted with chloroform (3×50 ml). The extract was dried over anhydrous sodium sulfate and the solvent was removed by vacuum evaporator. This resulted in an alcohol intermediate (III) appearing as a faintly yellow oil (9.4 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703799B2
Source datasetuspto-grants-2014_04
ORD IDord-c8b90d6f30ee4db8823e25314d0fb032
Source noteuspto-grants-2014_04