| Identification | Back Directory | [Name]
OXAZOLE-5-CARBOXYLIC ACID | [CAS]
118994-90-4 | [Synonyms]
5-Carboxy-1,3-oxazole oxazol-5-carboxylic acid 5-OXAZOLECARBOXYLIC ACID OXAZOLE-5-CARBOXYLIC ACID 5-Oxazolecarboxylicacid(9CI) 1,3-Oxazole-5-carboxylic acid Oxazole-5-carboxylic acid, 98+ 1,3-Oxazole-5-carboxylic acid 98% 5-Oxazolecarboxylic acid (9CI, ACI) | [Molecular Formula]
C4H3NO3 | [MDL Number]
MFCD04114931 | [MOL File]
118994-90-4.mol | [Molecular Weight]
113.07 |
| Chemical Properties | Back Directory | [Melting point ]
195-197 | [Boiling point ]
289.3±13.0 °C(Predicted) | [density ]
1.449±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
solid | [pka]
2.39±0.10(Predicted) | [color ]
Off-white to brown | [Water Solubility ]
Soluble in water. | [InChIKey]
QCGMEWVZBGQOFN-UHFFFAOYSA-N |
| Hazard Information | Back Directory | [Uses]
Decarboxylative cross-coupling of thiazole and oxazole-5-carboxylic acids with aryl halides is reported. | [Synthesis]
General procedure for the synthesis of oxazole-5-carboxylic acid from ethyl oxazole-5-carboxylate: an aqueous solution of lithium hydroxide monohydrate (124.5 kg, prepared by dissolving 49.44 kg of lithium hydroxide monohydrate in 319 kg of water, 398 mol) was slowly added to a solution of ethyl oxazole-5-carboxylate (54 kg, 382.7 mol) in water (54 kg), the reaction The temperature was kept below 25°C during the reaction. the reaction mixture was stirred for 6.5 h and then concentrated. Subsequently, an aqueous HCl solution (64.8 kg) was slowly added while keeping the temperature below 25°C. The mixture was cooled to 5°C and maintained for 1 h to promote crystallization. The crystalline product was collected by filtration, washed sequentially with cold water (88 kg) and isopropanol (171 kg) and finally dried under vacuum at 50 °C to give oxazole-5-carboxylic acid (37.88 kg, 87% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 13.68 (br.s, 1H), 8.59 (s, 1H), 7.88 (s, 1H). | [References]
[1] Patent: WO2016/193255, 2016, A1. Location in patent: Page/Page column 21 [2] Patent: WO2018/29126, 2018, A1. Location in patent: Page/Page column 49 |
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