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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975957Generated: November 2, 2026

3,5-Bis(trifluoromethyl)benzyl bromide → HCID 9872837, compound

https://huagongshe.com/reaction/1975957

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 11450797HCID 11450797—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9872837HCID 987283792%

Reaction Steps

To a solution of 0.074 g (0.21 mmol) 5-(2-chloro-phenyl)-N-methyl-2-(4-methyl-piperazin-1-yl)-isonicotinamide in 5 ml tetrahydrofuran at −10° C. were added dropwise 0.29 ml (0.29 mmol) of 1 M potassium hexamethyldisilazide solution in tetrahydrofuran. Stirring was continued for ½ h at −10° C. At this temperature 0.42 ml 3.5-bis(trifluormethyl)-benzylbromide were added. The reaction was quenched with water after 10 min and the mixture was extracted with three 15 ml portions of ethyl acetate. The combined organic layers were washed with brine, dried (magnesium sulfate) and evaporated. Chromatography of the residue afforded 0.113 g (92%) of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225316B1
Source datasetuspto-grants-2001_05
ORD IDord-ded54e33923346688cc242d1e47f2d00
Source noteuspto-grants-2001_05