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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040853Generated: November 1, 2026

Tert-butyl 3-oxopyrrolidine-1-carboxylate → tert-Butyl 3-methylidenepyrrolidine-1-carboxylate

https://huagongshe.com/reaction/2040853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
Reactant2-(4-Methylene-1-piperidyl)-3-nitropyridineHCID 57493809—
Producttert-Butyl 3-methylidenepyrrolidine-1-carboxylateHCID 15297967—

Reaction Steps

The title compound was synthesised following the method described here for Compound 2a using 1-Boc-3-pyrrolidinone instead of 1-(3-nitro-2-pyridyl)-4-oxopiperidine. After the usual work-up procedure, the crude product was purified by automated flash chromatography (Horizon®TM-Biotage) eluting with a Petroleum Ether-EtOAc gradient from 95:5 to 7:3, yielding the title compound as brownish oil. Yield: 75.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580962B2
Source datasetuspto-grants-2013_11
ORD IDord-4124b675ff494923995d5d1e4b097df0
Source noteuspto-grants-2013_11