Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486330Generated: October 25, 2026

4-Phenylsemicarbazide → 3-Hydroxy-2-[[(N-phenylaminocarbonyl)hydrazono]methyl]pyridine

https://huagongshe.com/reaction/486330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenylsemicarbazideHCID 10837—
Reactant3-HydroxypicolinaldehydeHCID 2737332—
SolventWater ethanolHCID 19096565—
Product3-Hydroxy-2-[[(N-phenylaminocarbonyl)hydrazono]methyl]pyridineHCID 13620718899%

Reaction Steps

4-Phenyl semicarbazide (4.91 g, 33 mmol) was added to a suspension of 3-hydroxy-2-pyridine carbaldehyde (4.0 g, 33 mmol) in a mixture of ethanol water (30 mL:40 mL). The reaction mixture was stirred at room temperature for 3 h and the yellow product was collected by filtration. The yellow precipitate was washed with EtOH/H2O 1:1 and dried under P2O5 to yield 8.22 g (99%) of product. It can be recrystallized from EtOH/H2O; m.p. 201°-2° C. (dec.). 1H NMR (d6 -DMSO) δ: 10.85 (br.s., 1H); 10.6 (br.s., 1H); 9.14 (s, 1H); 8.27 (s, 1H); 8.15 (d of d, 1H); 7.55 (d, 2H); 7.26-7.36 (m, 4H); 7.01 (t, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290942
Source datasetuspto-grants-1994_03
ORD IDord-1bee56f2f14144e0b3735674062c7c5c
Source noteuspto-grants-1994_03