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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737117Generated: October 31, 2026

Methyl iodide → HCID 57849642, compound

https://huagongshe.com/reaction/737117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDichloromethaneHCID 6344—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57849459HCID 57849459—
SolventAcetonitrileHCID 6342—
ProductHCID 57849642HCID 57849642—

Reaction Conditions

Temperature80 °C

Reaction Steps

This compound could be made the following manner: 100 mg of 3-phenyl-1-(2′-trifluoromethyl-biphenyl-4-ylmethyl)-piperazine would be dissolved in acetonitrile, 3 equiv. of N,N-diisopropylethylamine would be added followed by 1.1 equiv. of iodomethane. The reaction would be stirred at 80° C. overnight. The reaction would be diluted with dichloromethane and washed with 1N aqueous NaOH solution. The organic layer would be dried over Na2SO4, filtered and concentrated in vacuo. The crude residue would be purified by column chromatography to afford 1-methyl-2-phenyl-4-(2′-chloro-biphenyl-4-ylmethyl)-piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595397B2
Source datasetuspto-grants-2009_09
ORD IDord-8554b311924e44d383b55e535fc0c808
Source noteuspto-grants-2009_09