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HRID 25526作成日:2026年10月27日

4-Hydroxy-3-nitrobenzaldehyde → [5-(1H-Indol-2-yl)-2-methoxy-phenyl]-(4-hydroxy-3-nitro-benzyl)-amine

https://huagongshe.com/reaction/25526

反応式

関与物質

役割名称HCID仕込み量
反応物4-Hydroxy-3-nitrobenzaldehydeHCID 18169—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物5-(1H-indol-2-yl)-2-methoxy-phenylamineHCID 9900204—
溶媒Acetic AcidHCID 176—
溶媒DichloromethaneHCID 6344—
生成物[5-(1H-Indol-2-yl)-2-methoxy-phenyl]-(4-hydroxy-3-nitro-benzyl)-amineHCID 1029368739.4%

反応手順

4-Hydroxy-3-nitrobenzaldehyde (0.334 g, 2.0 mmol) was added to a stirred mixture of 5-(1H-indol-2-yl)-2-methoxy-phenylamine (0.476 g, 2.0 mmol) in methylene chloride (125 mL), followed by acetic acid (0.2 g). The resulting mixture was stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.46 g, 2.2 mmol) was added in one portion, and the resulting homogeneous solution was stirred at room temperature for 3 days. Saturoted aqueous sodium bicarbonate solution (100 mL) was added and the mixture was stirred for 2 hours. The mixture was shaken, the organic layer was separated and dried over Na2SO4. The solvent was evaporated to give a brown gum. Recrystallization from methanol gave the product (307 mg), mp 165-166° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858739B2
出典データセットuspto-grants-2005_02
ORD IDord-4a09980cb5f343ce9598f05e969b4d52
出典メモuspto-grants-2005_02