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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25523생성일: 2026년 10월 23일

3-Nitrobenzaldehyde → [5-(1H-indol-2-yl)-2-methoxy-phenyl]-(3-nitro-benzyl)-amine

https://huagongshe.com/ko/reaction/25523

반응식

참여 물질

역할이름HCID투입량
반응물3-NitrobenzaldehydeHCID 7449—
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]-(3-nitro-benzyl)-amineHCID 996955915.4%

반응 단계

3-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 3 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 oil. Recrystallization from ethyl acetate/hexane gave the product (115 mg), mp 160-162° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858739B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-d18519828ae54bcbb33480eea0e9956c
출처 메모uspto-grants-2005_02