HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526021Generated: October 28, 2026
3-Nitrobenzaldehyde → 5(4H)-Oxazolone, 2-methyl-4-[(3-nitrophenyl)methylene]-
https://huagongshe.com/reaction/526021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Product | 5(4H)-Oxazolone, 2-methyl-4-[(3-nitrophenyl)methylene]- | HCID 364504 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345680B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-2469baba46694a1abbabf634e57c6fc2 |
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| Source note | uspto-grants-2016_05 |
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