HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzoyl chloride → 5-(4-Chlorobenzoyl)-1, 2-dihydro-1-pyrrolizinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | 3H-1,2-dihydro-1-pyrrolizinone | HCID 97347 | — |
| Solvent | 1,1,1,2-Tetrachloroethane | HCID 12418 | — |
| Product | 5-(4-Chlorobenzoyl)-1, 2-dihydro-1-pyrrolizinone | HCID 54199234 | 72% |
Reaction Steps
To a stirred mixture of 12.1 g compound (1) and 8 g AICI3 in 40 ml tetrachloroethane was added dropwise 5.3 g 4-chlorobenzoyl chloride during 1 hour. The mixture was stirred at 40°-45° C. for 2 hours. The reaction mixture was added into 100 g ice-water. The organic layer was dried over MgSO4. Evaporated to dryness, 7 g crude product was obtained. Recrystallized from ethanol, 5.5 g of (3) was obtained as a white solid, mp 165°-166.5° C., yield 72%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616604 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-790094ec1bfb4f55b92d24e91ba4cfa8 |
| Source note | uspto-grants-1997_04 |