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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279662Generated: November 2, 2026

Ethyl 3-[1-benzyloxy-3-(isoamyloxycarbonyl)cyclobutan-3-yl]-4-nitrobutanoate → 4-[1-Benzyloxy-3-(isoamyloxycarbonyl)cyclobutan-3-yl]-2-pyrrolidone

https://huagongshe.com/reaction/1279662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-[1-benzyloxy-3-(isoamyloxycarbonyl)cyclobutan-3-yl]-4-nitrobutanoateHCID 18427813—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product4-[1-Benzyloxy-3-(isoamyloxycarbonyl)cyclobutan-3-yl]-2-pyrrolidoneHCID 18427809—

Reaction Conditions

Temperature50 °C

Reaction Steps

A 11.45 g (25.26 mmol) portion of crude ethyl 3-[1-benzyloxy-3-(isoamyloxycarbonyl)cyclobutan-3-yl]-4-nitrobutanoate was dissolved in 200 ml of ethanol to which was subsequently added 10 ml of Raney nickel under an atmosphere of nitrogen. After replacing nitrogen with hydrogen, this was stirred at 50° C. for 5 hours under an atmosphere of hydrogen. After cooling in an ice bath, the reaction solution was filtered through celite and then the solvent was evaporated under a reduced pressure to give 6.51 g (19.5 mmol) of the title compound. The thus obtained compound was used in the following reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448266B1
Source datasetuspto-grants-2002_09
ORD IDord-2de2fe1682a446bda0105d8fc41ec897
Source noteuspto-grants-2002_09