HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348271Generated: October 28, 2026
3-Bromobenzaldehyde → 2-(3-Bromophenyl)-4,5-dimethyloxazole-3-oxide
https://huagongshe.com/reaction/348271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | 2-Oxime 2,3-butanedione | HCID 6398969 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-(3-Bromophenyl)-4,5-dimethyloxazole-3-oxide | HCID 4087775 | 74.1% |
Reaction Steps
A solution of 2,3-butanedione monooxime (50 g, 0.49 mol) and 3-bromobenzaldehyde (101 g, 0.54 mol) in acetic acid (500 mL) was cooled to 0° C. and then gaseous HCl was bubbled through the solution for 35 min while the reaction was stirred in an ice bath. Diethyl ether (500 mL) was then added to the reaction to precipitate the product and the resultant slurry stirred 45 min at 0° C. before being filtered. The solids were rinsed with Et2O (50 mL), taken up in water (1 L) and concentrated NH4OH (60 mL) added to the slurry. This mixture was extracted with CHCl3, the organic layer was dried (MgSO4), and the solvent removed in vacuo to give 97.4 g (74%) of 2-(3-bromophenyl)-4,5-dimethyloxazole-3-oxide as a white solid. The compound should be used directly with 24–48 h.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176224B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-ee737189a9ad4ff5980d99110575a1c3 |
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| Source note | uspto-grants-2007_02 |
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