HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dimethoxyethane → N-Decyl-3-(3-[4-Methoxycarbonyl-2-oxo-pyrrolidino]phenyl)propenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | N-Decyl-3-[3-(4-carboxy-2-oxo-pyrrolidino)phenyl]propenamide | HCID 53878346 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-Decyl-3-(3-[4-Methoxycarbonyl-2-oxo-pyrrolidino]phenyl)propenamide | HCID 53968862 | — |
Reaction Steps
To a stirred mixture of 415 mg. of N-decyl-3-(3-[4-carboxy-2-oxo-pyrrolidino]phenyl)propenamide and 15 ml. of 1,2-dimethoxyethane is added a solution of 1.5 mmoles of diazomethane in 5 ml. of ether. The reaction mixture is stirred at room temperature for 16 hours, and then the excess diazomethane is decomposed by the addition of a few drops of acetic acid. The total solvents are removed by evaporation in vacuo, and the residue is dissolved in ethyl acetate. The ethyl acetate solution is washed with 1 N sodium hydroxide, followed by water, followed by saturated sodium chloride solution, and then dried using sodium sulfate. Evaporation of the dried ethyl acetate solution in vacuo affords the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04343813 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-7c295665dd2b46f7a2431202d095780c |
| Source note | uspto-grants-1982_08 |