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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441733Generated: October 27, 2026

Diethylamine → 4-(Diethylamino)-3-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/1441733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-3-(trifluoromethyl)benzonitrileHCID 10800647—
SolventDimethylacetamideHCID 31374—
Product4-(Diethylamino)-3-(trifluoromethyl)benzonitrileHCID 68677448—

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of 4-bromo-3-(trifluoromethyl)-benzonitrile (Yonezawa et al., Synthetic Communications (1996), 26, 1575-1578; 6.0 g, 24 mmol), diethylamine (8.3 mL, 80 mmol) and 25 mL N,N-dimethylacetamide is stirred in a tightly closed vessel for 16 hours at 135° C. After cooling, the reaction mixture is treated with a half-saturated aqueous solution of sodium hydrogen carbonate and extracted three times with ethyl acetate. The combined organic extracts are dried (Na2SO4) and the solvent is evaporated off under reduced pressure. The crude product is purified by column chromatography on silica gel, eluent hexane/ethyl acetate to give the title compound as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655669B2
Source datasetuspto-grants-2010_02
ORD IDord-dece2e21328944b8b1c8f36a9cc25562
Source noteuspto-grants-2010_02