HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → N-tert-butyl-5-methylisoxazole-3,4-dicarboximide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | HCID 10513407 | HCID 10513407 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-tert-butyl-5-methylisoxazole-3,4-dicarboximide | HCID 14990286 | 91.5% |
Reaction Steps
6.3 g )62.2 mmol) of methylmorpholine, 2.4 g (20 mmol) of dimethylaminopyridine and 14.6 g of a 50% strength solution of propanephosphonic anhydride (23 mmol) in dichloromethane were added dropwise in succession to 3.8 g (16.8 mmol) of 3-tert-butylaminocarbonyl-5-methylisoxazole-4-carboxylic acid in 150 ml of dichloromethane at -5° C. and the mixture was then refluxed for 6 hours. Working up was carried out as described above. 3.2 g (91%) of N-tert-butyl-5-methylisoxazole-3,4-dicarboximide were obtained as a solid of melting point 48°-50° C. (Example No. 2.001).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05378680 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-d303dc8ce49547a88a2c8381a24e0903 |
| Source note | uspto-grants-1995_01 |