Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichloroaniline | HCID 11123 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(2,5-dioxopyrrol-1-yl)propanoic acid | HCID 319936 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86746740 | HCID 86746740 | 35% |
Reaction Steps
A suspension of DL-2,5-dioxo-α-methyl-3-pyrroline-1-acetic acid (1.5 g, 0.0086 mol) in toluene is treated with thionyl chloride (1.28 mL, 0.0176 mol), warmed to 50° C., stirred for 2 1/2 hours, cooled and concentrated in vacuo to yield a yellow oil. The oil is dissolved in methylene chloride and added to a solution of 2,4-dichloroaniline (1.54 g, 0.0086 mol) and triethylamine (1.32 mL, 0.0094 mol) in methylene chloride under nitrogen at 0° C. The reaction mixture is stirred for 1 hour at room temperature and concentrated in vacuo to give a residue. The residue is flash chromatographed using hexane/ethyl acetate (80/20) as eluent on silica gel to give the title compound as a pale yellow solid (0.94 g, 35%, mp 131° C.), identified by 1HNMR, CIMS and IR analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05204366 |
|---|
| Source dataset | uspto-grants-1993_04 |
|---|
| ORD ID | ord-7ea860bacd6342bb8fff0fb10062ef09 |
|---|
| Source note | uspto-grants-1993_04 |
|---|