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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium PersulfateHCID 62655—
ReactantSodium AcetateHCID 517045—
Reactant2-Benzoyl-1-[3,3-di(ethoxycarbonyl)propyl]pyrroleHCID 14975130—
CatalystSilver NitrateHCID 24470—
CatalystManganese acetate tetrahydrateHCID 93021—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Productdiethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylateHCID 992857495.5%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082951
Source datasetuspto-grants-1992_01
ORD IDord-ed9ccb72c04b45c982da079b1f207cdb
Source noteuspto-grants-1992_01