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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632728Generated: October 31, 2026

3-(Trifluoromethyl)benzaldehyde → HCID 89445371, compound

https://huagongshe.com/reaction/632728

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzaldehydeHCID 67990—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantHCID 89442443HCID 89442443—
SolventAcetonitrileHCID 6342—
ProductHCID 89445371HCID 89445371—

Reaction Steps

In a round bottom flask equipped with a stir bar was dissolved 5-(4-Fluoro-phenyl)-6-piperazin-1-yl-pyrimidin-4-ylamine (1 eq) and 3-trifluoromethyl-benzaldehyde (1.05 eq) in acetonitrile. The vial was sealed with a rubber septa, then evacuated and backfilled with argon. To this sealed vessel was added trimethylsilyl cyanide (1.05 eq) and the reaction was allowed to stir at room temperature until complete. The reaction is quenched by addition of an equal amount of ammonium chloride (saturated, aqueous solution), then extracted with ethyl acetate. The organic layers are then dried over sodium sulfate, filtered and concentrated to give the title compound. LC-MS: (M+1=457, obsd.=457).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321760B2
Source datasetuspto-grants-2016_04
ORD IDord-39c2c078c0af47019cf0441dbfaf624f
Source noteuspto-grants-2016_04