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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090847Generated: October 31, 2026

Acetic Acid → diethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylate

https://huagongshe.com/reaction/1090847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetonitrileHCID 6342—
ReactantSodium AcetateHCID 517045—
ReactantHCID 53958697HCID 53958697—
CatalystManganese(3+)HCID 105130—
Catalystmanganese(III) acetate dihydrateHCID 160554—
SolventDiethyl EtherHCID 3283—
Productdiethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylateHCID 9928574—

Reaction Steps

To a warm, preferably 60°-80° C., mixture of a high valence metal ion, preferably a manganese(III) salt, and more preferably manganese(III) acetate, in an alkanoic acid, preferably acetic acid, or a polar aprotic solvent such as acetonitrile, is added a weak base, preferably sodium acetate, and a compound of formula IV, preferably 2-benzoyl-[3,3-di(ethoxycarbonyl)propyl]pyrrole. The reaction is stirred, preferably at 50°-70° C. until the reaction is complete. The reaction mixture is diluted with a polar solvent, such as diethyl ether, and filtered. The resulting solution is washed with water and aqueous base, preferably 10% sodium hydroxide, dried, and concentrated under reduced pressure. The product, a compound of formula I, preferably diethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylate, may be isolated by conventional means.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082951
Source datasetuspto-grants-1992_01
ORD IDord-87d775facd59459db77d8e10155f09cf
Source noteuspto-grants-1992_01