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HRID 12601作成日:2026年10月23日

2,4-Bis(trifluoromethyl)benzaldehyde → (NE)-N-[[2,4-bis(trifluoromethyl)phenyl]methylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/ja/reaction/12601

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Bis(trifluoromethyl)benzaldehydeHCID 2736095—
反応物Tert-ButanesulfinamideHCID 3382465—
触媒Copper SulfateHCID 24462—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(NE)-N-[[2,4-bis(trifluoromethyl)phenyl]methylidene]-2-methylpropane-2-sulfinamideHCID 178455562—

反応手順

A mixture of 2,4-bis trifluoromethyl benzaldehyde (10.0 g, 41.3 mmol), tert butyl sulfinamide (4.5 g, 37.2 mmol) and anhydrous CuSO4 (13.1 g, 82.6 mmol) in DCM (100 ml) was stirred at room temperature overnight. The fine suspension was diluted with water and extracted with DCM. The extracts were washed with water, dried (MgSO4) and evaporated in vacuo to afford the desired N-{(1E)-[2,4-bis(trifluoro methyl)phenyl]methylene}-2-methylpropane-2-sulfinamide as an off white solid (7.62 g, 53%), with no further purification. 1H NMR δ (ppm)(CDCl3): 8.99 (1 H, d, J=1.9 Hz), 8.35 (1 H, d, J=8.2 Hz), 8.02 (1 H, s), 7.92 (1 H, d, J=8.2 Hz), 1.28 (9 H, d, J=4.6 Hz); 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-d8a15633b09740b3a83773b2d22693a7
出典メモuspto-grants-2010_06