Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358613Generated: October 27, 2026

Methyl iodide → 2-Benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-benzamide

https://huagongshe.com/reaction/1358613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant2-Benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-benzamideHCID 9824373—
SolventDimethylformamideHCID 6228—
Product2-Benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-benzamideHCID 986842187%

Reaction Steps

To a solution of 100 mg (0.23 mmol) 2-benzyl-N-(3,5-bis-trifluoromethyl-benzyl)-benzamide in 1 ml N,N-dimethylformamide at 0° C. were added 50 mg (0.25 mmol) potassium hexamethyldisilazide. Stirring was continued for 1 h at this temperature and 0.016 ml (0.25 mmol) methyl iodide were added. After stirring for 3 h at room temperature, ethyl acetate was added. The mixture was washed with brine, dried (magnesium sulfate) and evaporated. The solvent was removed in vacuo and the residue was purified by flash chromatography to give 90 mg (87%) of the title compound as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596773B2
Source datasetuspto-grants-2003_07
ORD IDord-403329ad8e0949c3b6550edd634050ef
Source noteuspto-grants-2003_07