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HRID 25524作成日:2026年10月25日

4-Nitrobenzaldehyde → [5-(1H-Indol-2-yl)-2-methoxy-phenyl]-(4-nitro-benzyl)-amine

https://huagongshe.com/reaction/25524

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrobenzaldehydeHCID 541—
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-nitro-benzyl)-amineHCID 1029271438.8%

反応手順

4-Nitrobenzaldehyde (0.302 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 4 days. Saturated 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 an orange solid. Recrystallization from ethyl acetate gave the product (290 mg), mp 198-199° 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-cebbfcc888aa4162b8abe136e3ae7d6b
出典メモuspto-grants-2005_02