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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 711330생성일: 2026년 10월 25일

Methylamine → {[3,5-Bis(trifluoromethyl)phenyl]methyl}(methyl)amine

https://huagongshe.com/reaction/711330

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물1-(Chloromethyl)-3,5-bis(trifluoromethyl)benzeneHCID 123576—
용매MethanolHCID 887—
생성물{[3,5-Bis(trifluoromethyl)phenyl]methyl}(methyl)amineHCID 1095620440.9%

반응 조건

온도50 °C

반응 단계

Methylamine (3 g, 40% aqueous solution) was dissolved in 30 mL of MeOH. The reaction mixture was heated at 50° C. under stirring. 3,5-Bis(trifluoromethyl)-benzyl chloride (2 g, 7.6 mmol) dissolved in 10 mL of MeOH, was added. The solution was left stirring at this temperature for 5 h. The solution was concentrated carefully to remove MeOH as much as possible, then an aqueous solution of NaOH 1M was added and the aqueous layer was extracted with DCM. The two phases were separated; the organic phase was filtered through a phase separator and removed carefully in vacuo obtaining the title compound (0.8 g) as a yellow oil. UPLC-MS: m/z (ES+): 258.01 [M+H]+ Rt=0.60. 1H NMR (400 MHz, CDCl3) δ ppm 7.83 (s, 2H), 7.79 (s, 1H), 3.91 (s, 2H), 3.30 (m, 1H), 2.50 (s, 3H); UPLC-MS: Rt=1.30; m/z (ES+): 586 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181259B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-08bf3a079d804209965d1770ab8d4eb3
출처 메모uspto-grants-2015_11