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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968075Generated: October 25, 2026

Nitrogen → 1-(4-fluorophenyl)-2-(4-trifluoromethylphenyl)-N,N-dimethylethenylamine

https://huagongshe.com/reaction/968075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSodium hydrideHCID 24758—
Reactantp-Trifluoromethylbenzyl chlorideHCID 123096—
Reactant2-(4-fluorophenyl)-2-(N,N-dimethylamino)acetonitrileHCID 11309856—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(4-fluorophenyl)-2-(4-trifluoromethylphenyl)-N,N-dimethylethenylamineHCID 6974651088.3%

Reaction Steps

Into a 200 ml four-necked flask equipped with a thermometer, a stirrer, a dropping funnel and a N2 gas supply tube, a N2 gas was introduced so that the interior of the flask became a N2 atmosphere. 40 ml of dimethylformamide and 2.4 g (61.6 mmol) of sodium hydride (62% oil suspension) were charged, and a solution comprising 10 g (56 mmol) of 2-(4-fluorophenyl)-2-(N,N-dimethylamino)acetonitrile and 10.9 g (56 mmol) of 4-(trifluoromethyl)benzyl chloride, was dropwise added over a period of one hour at from 5 to 10° C. under cooling with ice water and then further reacted at from 20 to 30° C. for one hour. After completion of the reaction, 200 ml of water was added, and the mixture was extracted with 200 ml of ethyl acetate. The extract was washed with a 5% sodium hydrogen carbonate aqueous solution and water and then dried over anhydrous sodium sulfate. Ethyl acetate was distilled off, and the obtained oily substance was distilled under reduced pressure to obtain 15.3 g (yield: 88.3%) of the desired compound (boiling point: 130-135° C./0.6 KPa). The NMR spectrum data thereof were as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956132B2
Source datasetuspto-grants-2005_10
ORD IDord-b9e99094524b4150b3b6d134605baecb
Source noteuspto-grants-2005_10