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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388766Generated: October 26, 2026

Bromoacetonitrile → N-((1-(cyanomethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamide

https://huagongshe.com/reaction/388766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(piperidin-4-ylmethyl)-3,5-bis(trifluoromethyl)benzamideHCID 57993323—
SolventAcetonitrileHCID 6342—
ProductN-((1-(cyanomethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamideHCID 86636686—

Reaction Conditions

Temperature50 °C

Reaction Steps

N-(piperidin-4-ylmethyl)-3,5-bis(trifluoromethyl)benzamide (3.54 g, 10.0 mmol) was dissolved in CH3CN (100 mL). DIPEA (1.94 g, 15.0 mmol) and bromoacetonitrile (1.32 g, 11.0 mmol) were added. The reaction mixture was heated at 50° C. overnight. The solvent was removed in vacuo. Saturated NaHCO3 (40 mL) was added and the mixture was extracted with CH2Cl2 (4×30 mL). The combined organic solution was dried over anhydrous Na2SO4 and passed through a silica gel plug. The desired compound was eluted off with EtOAc. The product was further purified by crystallization from EtOAc/petroleum ether as a white solid (3.62 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377968B2
Source datasetuspto-grants-2013_02
ORD IDord-8e5b7e5f5da74fa8bfdeed53289e80a2
Source noteuspto-grants-2013_02