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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52195Generated: October 26, 2026

4-Chlorobenzoyl chloride → 5-(4-Chlorobenzoyl)-1, 2-dihydro-1-pyrrolizinone

https://huagongshe.com/reaction/52195

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
Reactant3H-1,2-dihydro-1-pyrrolizinoneHCID 97347—
Solvent1,1,1,2-TetrachloroethaneHCID 12418—
Product5-(4-Chlorobenzoyl)-1, 2-dihydro-1-pyrrolizinoneHCID 5419923472%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616604
Source datasetuspto-grants-1997_04
ORD IDord-790094ec1bfb4f55b92d24e91ba4cfa8
Source noteuspto-grants-1997_04