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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 53958697 | HCID 53958697 | — |
| Catalyst | Manganese(3+) | HCID 105130 | — |
| Catalyst | manganese(III) acetate dihydrate | HCID 160554 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | diethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05082951 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-87d775facd59459db77d8e10155f09cf |
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| Source note | uspto-grants-1992_01 |
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