Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 5-Formylaminomethyl-3-methylisoxazole | HCID 17932696 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19896738 | HCID 19896738 | — |
Reaction Steps
To a cooled and stirred solution of 5-formylaminomethyl-3-methylisoxazole (5.45 g, 39 mmol) and triethylamine (16.7 ml, 120 mmol) in dichloromethane (50 ml) was added dropwise phosphorus oxychloride (4 ml, 43 mmol) during 30 min., the temperature being kept below 0° C. Stirring was continued for 30 min., then a solution of sodium carbonate (4.55 g, 43 mmol) in water (50 ml) was added dropwise (<0° C.). Additional water (50 ml) was added and the layers were separated. The aqueous phase was extracted twice with dichloromethane (2×30 ml). The combined organic layers were dried, the solvent was evaporated, and the residue was extracted with ether (2×75 ml). The extracts were combined and the solvent was removed to give the title compound as a dark oil, 1H-NMR (CDCl3): 2.30 (s,3H), 4.75 (s,2H), 6.25 (s,1H). (Compound 16).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05116841 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-c8abfc48bfbc4bd3b03f57be767cd59d |
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| Source note | uspto-grants-1992_05 |
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