HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450062Generated: October 31, 2026
4-Nitrobenzaldehyde → 2-(4-Nitrophenyl)oxazole
https://huagongshe.com/reaction/450062
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2,2-Diethoxyethylamine | HCID 69524 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 2-(4-Nitrophenyl)oxazole | HCID 10976276 | 26.6% |
Reaction Steps
A mixture of p-nitro benzaldehyde (3 g, 19.8 mmol) and 2,2-diethoxy-ethylamine (2.64 g, 19.8 mmol) was heated at 100° C. for 2 hrs. The reaction mixture was cooled to room temperature and sulphuric acid (20 ml) was added. The resultant solution was added slowly to a mixture of phosphorus pentoxide (10 g) and sulphuric acid (3 ml) at 180° C. and the temperature was maintained for 30 min. The reaction mixture was cooled to room temperature and basified with saturated ammonium hydroxide solution. The resultant solid was filtered and recrystallised with ether to give 2-(4-nitro-phenyl)-oxazole (1 g, 26%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486962B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ef213a016b824419965d14640f2689a7 |
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| Source note | uspto-grants-2013_07 |
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