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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091993Generated: November 3, 2026

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

https://huagongshe.com/reaction/1091993

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 numberUS08129414B2
Source datasetuspto-grants-2012_03
ORD IDord-d9eba007f5e341d5abf57b6d84f5ca2a
Source noteuspto-grants-2012_03