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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25524생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/25524

반응식

참여 물질

역할이름HCID투입량
반응물4-NitrobenzaldehydeHCID 541—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물5-(1H-indol-2-yl)-2-methoxy-phenylamineHCID 9900204—
용매Acetic AcidHCID 176—
용매DichloromethaneHCID 6344—
생성물[5-(1H-Indol-2-yl)-2-methoxy-phenyl]-(4-nitro-benzyl)-amineHCID 1029271438.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858739B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-cebbfcc888aa4162b8abe136e3ae7d6b
출처 메모uspto-grants-2005_02