HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090856Generated: November 1, 2026
Water → diethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylate
https://huagongshe.com/reaction/1090856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylborane | HCID 7357 | — |
| Reactant | HCID 53682870 | HCID 53682870 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | diethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylate | HCID 9928574 | 75% |
Reaction Steps
To a solution of 2-benzoyl-[3-bromo-3,3-di(ethoxycarbonyl)propyl]pyrrole (436 mg, 1.0 mmol) in benzene (20 mL) was added triethylborane (1.0M in hexane, 5 mL, 5 mmol). The reaction mixture was stirred in an open vessel for one hour. Additional triethylborane (1 mL, 1 mmol) was added and the reaction was allowed to stir in an open vessel for an additional hour. The reaction mixture was poured into water and extracted with diethyl ether. The combined organic layers were washed with saturated aqueous sodium chloride, dried (Na2SO4), and concentrated under reduced pressure. The residue was purified by chromatography on silica gel eluting with hexane/ethyl acetate (85:15) to provide 266 mg (75%) 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-01d23d37945e4afaa583ab780fffc225 |
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| Source note | uspto-grants-1992_01 |
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