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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923384Generated: October 31, 2026

4-Nitrobenzaldehyde → Benzenemethanamine, 4-nitro-N-phenyl-

https://huagongshe.com/reaction/923384

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantAnilineHCID 6115—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductBenzenemethanamine, 4-nitro-N-phenyl-HCID 9695659.6%

Reaction Steps

Combined aniline (6.16 g, 66.2 mmol) and 4-nitrobenzaldehyde (10.0 g, 66.2 mmol) in MeOH (165 mL) and toluene (165 mL), and heated to 60° C. for 3 h. Cooled the mixture to room temperature, added sodium borohydride (5.01 g, 132 mmol) portionwise, and then stirred at room temperature for 1 h. Added sat NaHCO3 and stirred for 1 h. Added water and extracted with EtOAc. Combined extracts were washed with brine, dried (MgSO4) filtered, and evaporated to an amber oil that was purified by chromatography on silica gel, eluting with CH2Cl2 to give the title compound (9.0 g, 59.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278922B2
Source datasetuspto-grants-2016_03
ORD IDord-750157f6164245eb9402def8e65be9d0
Source noteuspto-grants-2016_03