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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411547Generated: October 30, 2026

Benzyl Chloride → 1-{8-[Benzyl(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl]-2,2,2-trifluoro-1-ethanone

https://huagongshe.com/reaction/411547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
Reactant2,2,2-Trifluoro-1-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]-1-ethanoneHCID 18540916—
SolventAcetonitrileHCID 6342—
Product1-{8-[Benzyl(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl]-2,2,2-trifluoro-1-ethanoneHCID 1854090342.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2,2,2-trifluoro-1-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]-1-ethanone (see step (v) above; 4.5 g, 16 mmol), benzylchloride (3.0 g, 16 mmol) and TEA (6.6 mL) in MeCN (50 mL) was stirred at 60° C. overnight. The mixture was evaporated and then DCM and water were added. The organic phase was washed with NaHCO3 solution, dried (Na2SO4) and then evaporated. The resulting crude product was purified by chromatography on silica gel (DCM eluant) to give 2.2 g (42%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559162B2
Source datasetuspto-grants-2003_05
ORD IDord-f69a2e1c55ec4e0a82eb4afc97c423e3
Source noteuspto-grants-2003_05