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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355589Generated: October 26, 2026

Sodium Chloride → 2-(Phenylmethyl)-2-azabicyclo[2.2.2]octane

https://huagongshe.com/reaction/1355589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant(4-Fluorobenzyl)triphenylphosphonium chlorideHCID 2733554—
Reactant2-Benzyl-2-azabicyclo[2.2.2]octan-6-oneHCID 12317473—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(Phenylmethyl)-2-azabicyclo[2.2.2]octaneHCID 12317470150.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a vigorously stirring suspension of p-fluorobenzyltriphenylphosphonium chloride (5.7 g, 14 mmol, Aldrich) in dry tetrahydrofuran (30 mL) at −78° C. was added 2.5 M n-butyllithium (4.7 mL, 12 mmol) in hexanes via syringe. After 30 min, the orange-yellow mixture was warmed to 0° C., and the suspension became deep red. After 5 min, 2-benzyl-2-azabicyclo[2.2.2]octan-6-one (1.2 g, 5.6 mmol) was added as a solution in dry tetrahydrofuran (25 mL) via cannula. Upon stirring vigorously for 2.5 hrs, the reaction was poured into saturated aqueous sodium chloride (70 mL), and the aqueous layer was extracted with ethyl acetate (3×70 mL). The combined organic layers were washed with saturated aqueous sodium chloride (50 mL), dried over sodium sulfate, and concentrated in vacuo. The resulting yellow solid was purified by flash chromatography (20%-70% ethyl acetate in hexanes) to yield 6-[4-fluorophenyl)methylene]-2-(phenylmethyl)-2-azabicyclo[2.2.2]octane (1.7 g, 99%) as a pale yellow oil. MS (ESI) 308 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586446B1
Source datasetuspto-grants-2003_07
ORD IDord-f66f5f4791a346c394103634f3a9fed3
Source noteuspto-grants-2003_07