Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 11323027 | HCID 11323027 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(2-Methoxy-4-nitrophenyl)oxazole | HCID 10198340 | — |
| Product | HCID 11323027 | HCID 11323027 | — |
Reaction Steps
5-(2-Methoxy-4-nitrophenyl)-4-oxazolecarboxylic acid was prepared in the same manner as in Example 1-(1) and (2), and the resulting wet cake was dried. The dried product (13.2 g, 0.05 mol) was dissolved in 130 g of DMF. Water (66 g) was added thereto, and the solution was heated at 90° C. for 9 hours for decarboxylation. After cooling, 31 g of water was added to the reaction mixture. The mixture was stirred for 30 minutes, and the precipitate was collected by filtration to give 7.6 g (76% based on the 5-(2-methoxy-4-nitrophenyl)-4-oxazolecarboxylic acid) of the title compound as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06423849B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-15ccb324d25c43bb94cd1a2e59a709a1 |
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| Source note | uspto-grants-2002_07 |
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