Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1,3-Oxazole-4-carboxylic acid | HCID 14281430 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86687688 | HCID 86687688 | 97% |
Reaction Steps
In a 10-mL round bottom flask under N2 were dissolved 4-oxazolecarboxylic acid (500 mg, 4.42 mmol) and oxalyl chloride (1.94 mL, 22.1 mmol) with 2 drop of DMF in 10 mL of DCM. The reaction was stirred at rt for 2 h. The reaction mixture was concentrated under reduced pressure and the material was carried forward crude. Under N2, oxazole-4-carbonyl chloride (crude) was dissolved in 10 mL of acetone and treated at 0° C. with a solution of sodium azide (575 mg, 8.84 mmol) in 1.0 mL of water. After 1 h, the reaction mixture was diluted with AcOEt then neutralized with H2O. The aqueous phase was extracted 3× with AcOEt then the organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. The crude oxazole-4-carbonyl azide (590 mg, 4.27 mmol, 97% yield) was carried forward without further purification into the next step. MS (ESI, positive ion) [M+1]+: 139.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012443B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-5824d11c11d74bf1afe1a03a26f713e8 |
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| Source note | uspto-grants-2015_04 |
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