HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-ethoxycarbonyl-1,2,3,6-tetrahydrophtalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,2,3,6-Tetrahydrophthalimide | HCID 6808 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-ethoxycarbonyl-1,2,3,6-tetrahydrophtalimide | HCID 23628680 | 82% |
Reaction Steps
Ethyl chloroformate (0.18 ml, 1.89 mmol) was added dropwise to a stirred solution of 1,2,3,6-tetrahydrophthalimide (0.22 g, 1.45 mmol) and triethylamine (0.23 ml, 1.67 mmol) in dimethylformamide (2 ml) at 0-5° C. The reaction mixture was allowed to warm to room temperature and stand for 4 h. Methyl alcohol (1 ml) was added, diluted with chloroform (20 ml) and washed with water (3×10 ml). The chloroform solution was dried (Na2SO4) and concentrated in vacuum to give N-ethoxycarbonyl-1,2,3,6-tetrahydrophthalimide (yield 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273304B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-e657a01ad393477aad2b02d99c9d7b06 |
| Source note | uspto-grants-2016_03 |