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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046548Generated: October 26, 2026

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

https://huagongshe.com/reaction/1046548

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 numberUS08569344B2
Source datasetuspto-grants-2013_10
ORD IDord-0203ba48e9c64d0bba9466732afb5cc3
Source noteuspto-grants-2013_10