HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020343Generated: November 2, 2026
Hydrochloric Acid → 2-Bromo-4-(trifluoromethyl)-1,3-oxazole-5-carboxylic acid
https://huagongshe.com/reaction/1020343
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Ethyl 2-bromo-4-(trifluoromethyl)-1,3-oxazole-5-carboxylate | HCID 53403202 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | 2-Bromo-4-(trifluoromethyl)-1,3-oxazole-5-carboxylic acid | HCID 57461789 | 88.3% |
Reaction Steps
LiOH.H2O (0.64 g, 15.25 mmol) was added to a solution of ethyl 2-bromo-4-trifluoromethyloxazole-5-carboxylate (A-2) (3.50 g, 12.2 mmol) in THF/H2O (20/5 mL) at 0° C. followed by stirring for 3 h at 0° C. The reaction mixture was diluted with EtOAc/H2O (25/25 mL) and neutralized with 1 M HCl (16 mL) at 0° C. The organic phase was separated, dried over MgSO4, filtered, and concentrated. The product was dried in vacuo to yield 2-bromo-4-trifluoromethyloxazole-5-carboxylic acid (A-38) as a white solid (2.80 g, 88% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716312B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-19fd433f5dfc4a29a3f71291672a81eb |
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| Source note | uspto-grants-2014_05 |
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