HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337686Generated: October 31, 2026
Sodium ethoxide → HCID 131732035, compound
https://huagongshe.com/reaction/337686
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 131732034 | HCID 131732034 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131732035 | HCID 131732035 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889714B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-b9e72903077d43998452d7b6475c3250 |
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| Source note | uspto-grants-2014_11 |
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