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HRID 1039416作成日:2026年10月27日

1,2-Dichloroethane → 5-Acetyl-2-methoxy-N-[[4-(trifluoromethyl)phenyl]methyl]benzamide

https://huagongshe.com/reaction/1039416

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物4-(Trifluoromethyl)benzylamineHCID 76804—
反応物5-Acetyl-2-methoxybenzoic acidHCID 18954591—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物5-Acetyl-2-methoxy-N-[[4-(trifluoromethyl)phenyl]methyl]benzamideHCID 21964535—

反応手順

To a stirred solution of 2-Methoxy-5-acetylbenzoic acid (Step B, 2.5 g, 12.8 mmol), HOBt.H20 (2.08 g, 15.4 mmol), and EDC (3.70 g, 19.3 mmol) in CH2Cl2 (20 ml) and DMF (5 ml) was added 4-(Trifluoromethyl)benzylamine (2.48 g, 14.1 mmol), and the mixture was stirred for 16 hours at room temperature. The reaction mixture was concentrated under reduced pressure and then redissolved in ethyl acetate. The organic layer was washed with 3% K2CO3, 1 N HCl, and brine, dried over Na2SO4, filtered and concentrated. The purification was done by flash chromatography on silica gel column (chloroform:methanol 95:5) to provide the title compound as white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08552062B2
出典データセットuspto-grants-2013_10
ORD IDord-80ea8464b6ca4da2ae704341cd72a5c4
出典メモuspto-grants-2013_10