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HRID 85095作成日:2026年10月27日

o-(Trifluoromethyl)benzaldehyde → 2-(2-(trifluoromethyl)phenyl)-1H-benzo[d]imidazole-4-carboxylic acid

https://huagongshe.com/reaction/85095

反応式

関与物質

役割名称HCID仕込み量
反応物o-(Trifluoromethyl)benzaldehydeHCID 123067—
反応物2,3-Diaminobenzoic acidHCID 198069—
反応物Sodium PyrosulfiteHCID 656671—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-(2-(trifluoromethyl)phenyl)-1H-benzo[d]imidazole-4-carboxylic acidHCID 6720160274.2%

反応条件

温度100 °C

反応手順

2,3-diaminobenzoic acid (1; 50 mg, 0.33 mmol), 2-(trifluoromethyl)benzaldehyde (2; 57 mg, 0.33 mmol), and sodium metabisulfite (Na2S2O5, 82 mg, 0.43 mmol) were taken up in DMF (5 mL) and stirred at 100° C. for 17 h. The reaction mixture was cooled to room temperature and diluted with H2O. The resulting mixture was stirred at room temperature for 1 h and filtered. The collected solids were washed with water and dried to afford 2-(2-(trifluoromethyl)phenyl)-1H-benzo[d]imidazole-4-carboxylic acid 3 as a pale brown solid (75 mg, yield: 74%). MS (ESI) calcd for C15H9F3N2O2: 306.06; found: 307 [M+H].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846947B2
出典データセットuspto-grants-2014_09
ORD IDord-b3298b89d23c40499eca393070544e95
出典メモuspto-grants-2014_09