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HRID 12602作成日:2026年10月27日

2,5-Bis(trifluoromethyl)benzaldehyde → (NE)-N-[[2,5-bis(trifluoromethyl)phenyl]methylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/12602

反応式

関与物質

役割名称HCID仕込み量
反応物2,5-Bis(trifluoromethyl)benzaldehydeHCID 2737807—
反応物Tert-ButanesulfinamideHCID 3382465—
触媒Copper SulfateHCID 24462—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(NE)-N-[[2,5-bis(trifluoromethyl)phenyl]methylidene]-2-methylpropane-2-sulfinamideHCID 5798748991%

反応手順

A mixture of 2,5-bis trifluoromethyl benzaldehyde (21.5 g, 88.8 mmol), tert butyl sulfinamide (16.1 g, 133 mmol) and anhydrous CuSO4 (16.5 g, 103 mmol) in DCM (94 ml) was stirred at room temperature for 16 hours and at reflux for 3 days. The fine suspension was diluted with water and extracted with DCM. The extracts were washed with water, dried (MgSO4) and evaporated in vacuo to an off white solid which was purified by chromatography (silica, 4-10% EtOAc/isohexane) to give the desired N-{(1E)-[2,5-bis(trifluoromethyl)phenyl]methylene}-2-methylpropane-2-sulfinamide as a white crystalline solid (14.8 g, 91%); 1H NMR δ (ppm)(CDCl3): 8.98 (1 H, d, J=1.8 Hz), 8.46 (1 H, s), 7.92-7.85 (2 H, m), 1.29 (9 H, s); m/z (ES+) 346 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728022B2
出典データセットuspto-grants-2010_06
ORD IDord-bcbee99499544c32b5f10b72d55104b4
出典メモuspto-grants-2010_06