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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25524Generated: October 25, 2026

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

https://huagongshe.com/reaction/25524

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-(1H-indol-2-yl)-2-methoxy-phenylamineHCID 9900204—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product[5-(1H-Indol-2-yl)-2-methoxy-phenyl]-(4-nitro-benzyl)-amineHCID 1029271438.8%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858739B2
Source datasetuspto-grants-2005_02
ORD IDord-cebbfcc888aa4162b8abe136e3ae7d6b
Source noteuspto-grants-2005_02