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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Bromomethyl)-1-fluoro-4-(trifluoromethyl)benzeneHCID 2737571—
SolventDiethyl EtherHCID 3283—
Product1-Benzyl-4-[2-fluoro-5-(trifluoromethyl)benzyl]piperidin-4-olHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449475B2
Source datasetuspto-grants-2008_11
ORD IDord-cc5e2a82d42b4024ada4b9feecfc3c3b
Source noteuspto-grants-2008_11