HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270040Generated: October 31, 2026
Iodine → 1-Benzyl-4-[2-fluoro-5-(trifluoromethyl)benzyl]piperidin-4-ol
https://huagongshe.com/reaction/270040
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(Bromomethyl)-1-fluoro-4-(trifluoromethyl)benzene | HCID 2737571 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Benzyl-4-[2-fluoro-5-(trifluoromethyl)benzyl]piperidin-4-ol | HCID 68962482 | — |
Reaction Steps
To a stirring suspension of Mg strips (308 mg) in Et2O (5 mL) was added a crystal of iodine followed by 0.3 mL of 2-(bromomethyl)-1-fluoro-4-(trifluoromethyl)benzene under argon. The reaction was initiated with a high intensity heat gun, then 2-(bromomethyl)-1-fluoro-4-(trifluoromethyl)benzene (2.5 g, 9.73 mmol) in Et2O (5 mL) was added slowly (maintaining reflux). After addition was completed the reaction mixture was refluxed for 50 min, cooled to room temperature. A solution of 1-benzylpiperidin-4-one (1.84 g, 9.73 mmol) in Et2O (10 mL) was added slowly with vigorous stirring. After addition was completed, the reaction mixture was left at room temperature for 50 min, saturated aqueous NH4Cl solution was added and stirred at room temperature untill hydrolysis was finished, extracted with ethyl acetate. The combined organic layer was washed with water, dtied over Na2SO4, filtered and concentrated. The residue was purified by silica gel flash chromatography (0-1% methanol in dichloromethane, 0.2% NH4OH) to give the subtitled compound (720 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449475B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-cc5e2a82d42b4024ada4b9feecfc3c3b |
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| Source note | uspto-grants-2008_11 |
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