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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337676Generated: October 29, 2026

Sodium ethoxide → HCID 131732025, compound

https://huagongshe.com/reaction/337676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
Reactantcis-1-(1,1-Dimethylethyl) 3-ethyl 4-(4-pyridinyl)-1,3-piperidinedicarboxylateHCID 131732024—
SolventEthanolHCID 702—
ProductHCID 131732025HCID 131732025—

Reaction Conditions

Temperature60 °C

Reaction Steps

To an ethanol solution (0.4 M) of cis-1-(1,1-dimethylethyl) 3-ethyl 4-(4-pyridinyl)-1,3-piperidinedicarboxylate (1 eq.) from the previous step was added freshly prepared sodium ethoxide (1.1 eq.). The resulting yellow-orange solution was heated at 60° C. for 12 h. The volatiles were then removed in vacuo and the residue was partitioned between EtOAc and sat. aq. NH4Cl. The aqueous layer was separated and back-extracted with EtOAc. The combined organic extracts were washed further with water and brine, dried over Na2SO4, treated with activated charcoal, filtered and the filtrate concentrated in vacuo. Purification of the crude product thus obtained by way of column chromatography (SiO2, 80:20 (v/v) Hex:EtOAc→EtOAc) afforded the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-9098857d8786483296308cef6a327b6d
Source noteuspto-grants-2014_11