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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 508626Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/508626

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromoacetonitrileHCID 11534—
EduktDiisopropylethylamineHCID 81531—
EduktN-(piperidin-4-ylmethyl)-3,5-bis(trifluoromethyl)benzamideHCID 57993323—
LösungsmittelAcetonitrileHCID 6342—
ProduktN-((1-(cyanomethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamideHCID 86636686—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096522B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-e6b1bc3ae9eb40999b2fabeb7d6cc954
Quellennotizuspto-grants-2015_08