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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848434Generated: October 30, 2026

Tert-butyl 4-(2-ethoxy-2-oxoethyl)-4-(nitromethyl)piperidine-1-carboxylate → Tert-butyl 3-oxo-2,8-diazaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/1848434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(2-ethoxy-2-oxoethyl)-4-(nitromethyl)piperidine-1-carboxylateHCID 86709442—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductTert-butyl 3-oxo-2,8-diazaspiro[4.5]decane-8-carboxylateHCID 10015184—

Reaction Steps

A mixture of tert-butyl 4-(2-ethoxy-2-oxoethyl)-4-(nitromethyl)piperidine-1-carboxylate (330 g, 990 mmol, 1.00 equiv, 99%) and Ni (40 g, 0.15 equiv) in ethanol (1200 mL) was stirred for 24 h under a hydrogen atmosphere at room temperature. The solid was filtered out. The filtrate was concentrated under vacuum. The crude product was purified by re-crystallization from ether to afford the title compound. LC-MS (ES, m/z): 199 [M+H]+; H-NMR (400 MHz, CDCl3, ppm): 1.447-1.476 (9H, s), 1.597-1.673 (4H, m, J=30.4 Hz), 2.235 (2H, s), 3.226 (2H, s), 3.284-3.348 (2H, m, J=25.6 Hz), 3.507-3.567 (2H, m, J=24 Hz), 6.048 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952166B2
Source datasetuspto-grants-2015_02
ORD IDord-703d2dcbc635414ca5c143e76924f308
Source noteuspto-grants-2015_02