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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337686Generated: October 31, 2026

Sodium ethoxide → HCID 131732035, compound

https://huagongshe.com/reaction/337686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 131732034HCID 131732034—
SolventEthanolHCID 702—
ProductHCID 131732035HCID 131732035—

Reaction Conditions

Temperature55 °C

Reaction Steps

To an ethanol solution (0.1 M) of cis-1-(1,1-dimethylethyl) 3-ethyl 4-(3-{[(methyloxy)methyl]oxy}-4-pyridinyl)-1,3-piperidinedicarboxylate (1 eq.) from the previous step was added freshly prepared sodium ethoxide (1.2 eq.). The resulting yellow-orange solution was heated at 55° C. for 16 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, filtered and the filtrate concentrated in vacuo. Purification of the crude product thus obtained by way of column chromatography (SiO2, 95:5 (v/v) Hex:EtOAc→1:1 (v/v) Hex: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-b9e72903077d43998452d7b6475c3250
Source noteuspto-grants-2014_11