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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019773Generated: November 1, 2026

4-Fluorobenzylamine → Benzeneethanamine, N-[(4-fluorophenyl)methyl]-3-nitro-

https://huagongshe.com/reaction/1019773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzylamineHCID 67326—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(3-nitrophenyl)acetaldehydeHCID 11528408—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductBenzeneethanamine, N-[(4-fluorophenyl)methyl]-3-nitro-HCID 6746891140%

Reaction Steps

2-(3-nitrophenyl)acetaldehyde (1.2 g, 7.33 mmol) was dissolved in methanol (50 mL) and 4-fluorobenzylamine (1.88 g, 14.67 mmol) was added at 15° C. followed by 1-2 drops of glacial acetic acid. The reaction was stirred at room temperature for 2 hours then sodium borohydride (0.14 g, 3.6 6 mmol) was added in lots at 0-10° C. and the solution allowed to warm to room temperature and stirred for a further 2 hours. The reaction mixture was poured into sodium bicarbonate solution (75 mL) and stirred for 15 minutes. The mixture was extracted with EtOAc (2×60 mL) then the combined organic extracts were washed with brine (50 mL) and dried (Na2SO4). The solvents were removed under reduced pressure to afford the crude compound which was purified by column chromatography on neutral silica gel using 1-2% methanol in DCM to afford the title compound (0.793 g, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716287B2
Source datasetuspto-grants-2014_05
ORD IDord-83485fe24e5247f49a23b076e4a07433
Source noteuspto-grants-2014_05