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HRID 220737作成日:2026年10月26日

Toluene → 4-Methyl-1-(4-(trifluoromethyl)phenyl)pentan-1-one

https://huagongshe.com/reaction/220737

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物TetrahydrofuranHCID 8028—
反応物1-BromopentaneHCID 8057—
反応物Benzonitrile, 4-(trifluoromethyl)-HCID 67995—
反応物MagnesiumHCID 5462224—
溶媒WaterHCID 962—
生成物4-Methyl-1-(4-(trifluoromethyl)phenyl)pentan-1-oneHCID 46941396—

反応手順

Magnesium (17 g) was stirred 10 min under nitrogen then THF (400 mL) was added. 1-Bromo-4 -methylbutane (5 mL) was added and the mixture stirred 5 min until the reaction initiated (exotherm) the reminder of the bromomethylbutane (100 g, 0.672 mol) was added keeping the temp below 35° C. (water bath). The mixture was stirred 1 hr at RT and a solution of 4-trifluoromethylbenzonitrile (100 g, 0.584 mol) in toluene (1 L) containing some CuBr was added dropwise keeping the temp 25° C. The solution was stirred 1 h and quenched carefully with 15% H2SO4 (exotherm). The organic layer was decanted, washed with brine, dried over (MgSO4) and concentrated in vacuo. The oil was purified by column chromatography on silica using isohexane as eluant to give 4-methyl-1-[4-(trifluoromethyl)phenyl]pentan-1-one (126 g) which solidified on standing. 1H NMR δ (ppm)(CDCl3): 8.06 (2H, d, J 8.1 Hz), 7.73 (2H, d, J 8.1 Hz), 2.99 (2H, app. t, J 7.4 Hz), 1.68-1.60 (3H, m), 0.96 (6H, d, J 6.3 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08203004B2
出典データセットuspto-grants-2012_06
ORD IDord-2abcdfc4e3864f97a79dfbc0f8bf4cac
出典メモuspto-grants-2012_06