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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184501Generated: October 31, 2026

Ethyl 4-(4-oxopiperidin-1-yl)benzoate → Ethyl 4-(4-methylenepiperidin-1-yl)benzoate

https://huagongshe.com/reaction/1184501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-(4-oxopiperidin-1-yl)benzoateHCID 12717442—
Reactant4-Methylene-1-phenylpiperidineHCID 58902724—
ProductEthyl 4-(4-methylenepiperidin-1-yl)benzoateHCID 16109082—

Reaction Steps

Using ethyl 4-(4-oxopiperidin-1-yl)benzoate 390B (0.575 g, 2.325 mmol), Wittig olefination was carried out as described for 389A. The title compound was obtained as an off-white crystalline solid (0.338 g, 59.3% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.21-1.38 (m, 3H) 2.18-2.30 (m, 4H) 3.37-3.50 (m, 4H) 4.23 (q, J=7.16 Hz, 2H) 4.78 (s, 2H) 6.95-7.04 (m, 2H) 7.72-7.82 (m, 2H). ESI-MS: m/z 246.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669249B2
Source datasetuspto-grants-2014_03
ORD IDord-de179ae5883e4eb697938a6038e5d41c
Source noteuspto-grants-2014_03