HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090855Generated: November 1, 2026
Acetic Anhydride → diethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylate
https://huagongshe.com/reaction/1090855
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Persulfate | HCID 62655 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-Benzoyl-1-[3,3-di(ethoxycarbonyl)propyl]pyrrole | HCID 14975130 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Catalyst | Manganese acetate tetrahydrate | HCID 93021 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | diethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylate | HCID 9928574 | 95.5% |
Reaction Steps
A mixture of manganese(II) acetate tetrahydrate (343 mg, 1.40 mmol), silver nitrate (23.8 mg, 0.140 mmol), sodium acetate (420 mg, 5 mmol), acetic anhydride (542 mg, 4.20 mmol) and sodium persulfate (333 mg, 1.4 mmol) in acetic acid (8 mL) was stirred at 80° C. for 30 minutes. To this mixture was added a solution of 2-benzoyl-1-[3,3-di(ethoxycarbonyl)propyl]pyrrole (500 mg, 1.40 mmol) in acetic acid (2 mL). To the reaction mixture was then added additional sodium persulfate (333 mg, 1.4 mmol). The resulting mixture was stirred at 80° C. for 12 hours, cooled, poured into water (25 mL), and extracted with toluene (3×25 mL). The combined toluene extracts were washed with water (25 mL) and concentrated under reduced pressure, providing 475 mg (95%) of diethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylate.
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-ed9ccb72c04b45c982da079b1f207cdb |
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| Source note | uspto-grants-1992_01 |
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