HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-ethoxycarbonyl-2,3-dimethylmaleimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2,3-Dimethylmaleimide | HCID 28793 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-ethoxycarbonyl-2,3-dimethylmaleimide | HCID 23628596 | 80% |
Reaction Steps
Ethyl chloroformate (1.5 ml, 15.6 mmol) was added dropwise to a stirred solution of 2,3-dimethylmaleimide (1.5 g, 12 mmol) and triethylamine (2 ml, 14 mmol) in dimethylformamide (10 ml) at 0-5° C. The reaction mixture was allowed to warm to room temperature and stand for 4 h. Methyl alcohol (10 ml) was added, diluted with chloroform (50 ml) and washed with water (3×20 ml). The chloroform solution was dried (Na2SO4) and concentrated in vacuum to give N-ethoxycarbonyl-2,3-dimethylmaleimide (yield 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273304B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-c9815ff0ad7f4f5e9e8fdb8fcb054b56 |
| Source note | uspto-grants-2016_03 |