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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692162Generated: October 31, 2026

3-Nitrobenzaldehyde → 5(4H)-Oxazolone, 2-methyl-4-[(3-nitrophenyl)methylene]-

https://huagongshe.com/reaction/1692162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
ReactantAcetic AnhydrideHCID 7918—
ReactantAcetylglycineHCID 10972—
ReactantSodium AcetateHCID 517045—
Product5(4H)-Oxazolone, 2-methyl-4-[(3-nitrophenyl)methylene]-HCID 36450478%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-Nitrobenzaldehyde (45.3 g, 0.3 mol), N-acetylglycine (42.1 g, 0.36 mol) and sodium acetate (32 g, 0.39 mol) were mixed with acetic anhydride (142 ml, 1.5 mol) and the resulting mixture heated with stirring to 120° C. for 6 hrs, giving a dark solution. The mixture was then cooled to RT overnight, resulting in the formation of a precipitated solid. The reaction mixture was poured into ice-water (130 g) and the resulting suspended solid was collected by filtration. The crude solid product (72 g) was washed with acetone (80 ml) then recrystallized from hot acetone (320 ml) to give a crystalline solid that was washed with 50% aqueous ethanol, then dried at 40° C./40 mmHg to give 2-methyl-4-(3-nitrobenzylidene)oxazol-5(4H)-one (49.0 g, 78%) as pale yellow needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153841B2
Source datasetuspto-grants-2012_04
ORD IDord-89d4337c0c86403d86f6955978dc2c56
Source noteuspto-grants-2012_04