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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855143Generated: November 3, 2026

Ethyl (S)-2-(Boc-amino)-6-diazo-5-oxohexanoate → (S)-1-tert-butyl 2-ethyl 5-oxopiperidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1855143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (S)-2-(Boc-amino)-6-diazo-5-oxohexanoateHCID 86700661—
SolventDichloromethaneHCID 6344—
Product(S)-1-tert-butyl 2-ethyl 5-oxopiperidine-1,2-dicarboxylateHCID 7070116655%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of (S)-ethyl 2-((tert-butoxycarbonyl)amino)-6-diazo-5-oxohexanoate (350 g, 1.18 mol) in DCM (1500 mL) was added to a solution of Rh2(OAc)4 (3.5 g, 7.9 mmol) in DCM (750 mL) at 0° C. The reaction was then stirred at 20° C. overnight and then concentrated in vacuum. The crude sample was purified by silica gel column chromatography (5:1 petroleum ether/EtOAc) to afford (S)-1-tert-butyl 2-ethyl 5-oxopiperidine-1,2-dicarboxylate (175.9 g, 55%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962843B2
Source datasetuspto-grants-2015_02
ORD IDord-bf5d6917e5d3475ebbb8ea51c69c30f8
Source noteuspto-grants-2015_02