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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 968075생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/968075

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Sodium hydrideHCID 24758—
반응물p-Trifluoromethylbenzyl chlorideHCID 123096—
반응물2-(4-fluorophenyl)-2-(N,N-dimethylamino)acetonitrileHCID 11309856—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(4-fluorophenyl)-2-(4-trifluoromethylphenyl)-N,N-dimethylethenylamineHCID 6974651088.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06956132B2
출처 데이터셋uspto-grants-2005_10
ORD IDord-b9e99094524b4150b3b6d134605baecb
출처 메모uspto-grants-2005_10