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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Bicyclo(2.2.1)heptan-2-one | HCID 10345 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Fluorophenyl)bicyclo[2.2.1]heptan-2-ol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703799B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-c8b90d6f30ee4db8823e25314d0fb032 |
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| Source note | uspto-grants-2014_04 |
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