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HRID 711330作成日:2026年10月26日

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

https://huagongshe.com/reaction/711330

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物1-(Chloromethyl)-3,5-bis(trifluoromethyl)benzeneHCID 123576—
溶媒MethanolHCID 887—
生成物{[3,5-Bis(trifluoromethyl)phenyl]methyl}(methyl)amineHCID 1095620440.9%

反応条件

温度50 °C

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181259B2
出典データセットuspto-grants-2015_11
ORD IDord-08bf3a079d804209965d1770ab8d4eb3
出典メモuspto-grants-2015_11