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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25523Generated: October 26, 2026

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

https://huagongshe.com/reaction/25523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
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]-(3-nitro-benzyl)-amineHCID 996955915.4%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858739B2
Source datasetuspto-grants-2005_02
ORD IDord-d18519828ae54bcbb33480eea0e9956c
Source noteuspto-grants-2005_02