HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Propylpyrrolidine-2,4-dione → HCID 19895507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Propylpyrrolidine-2,4-dione | HCID 13560383 | — |
| Reactant | HCID 14074904 | HCID 14074904 | — |
| Reactant | HCID 19895520 | HCID 19895520 | — |
| Reactant | Toluene water | HCID 22272177 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Propylpyrrolidine-2,4-dione | HCID 13560383 | — |
| Product | HCID 19895507 | HCID 19895507 | 94% |
Reaction Steps
Freshly prepared 1-propyl-2,4-dioxopyrrolidine was prepared as described in Example 1e from 3-carboethoxy-1-propyl-2,4-dioxopyrrolidine (3.55 g) in acetonitrile (100 ml). The 1-propyl-2,4-dioxopyrrolidine was mixed with methyl 3-amino-2-pentylthiophene-4-carboxylate (2.70 g) in toluene (65 ml). The mixture was refluxed for 2 hours with removal of the water/toluene azeotrope using a Dean-Stark trap. After distilling off the excess toluene, the residue was taken up in ethyl acetate, washed sequentially with saturated aqueous Na2CO3 and brine, then dried (Na2SO4) and concentrated. Chromatographic purification over silica gel afforded the title product (3.92 g, 94%) as a yellow oil; tlc, Rf =0.12, silica gel, ethyl acetate:hexane (1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04975435 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-adfe987bd3554d20b65115943ffda4e8 |
| Source note | uspto-grants-1990_12 |