Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Malonate Ion | HCID 9084 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Propanedioic acid, monoethyl ester | HCID 3595298 | — |
| Reactant | 4-Piperidinol, 1-(2-methoxyethyl)- (9CI) | HCID 21353752 | — |
| Reactant | HCID 86761020 | HCID 86761020 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69018590 | HCID 69018590 | 45.2% |
Reaction Steps
To a solution of 1-(2-Methoxy-ethyl)-piperidin-4-ol (5.74 mmol) in THF (20 mL) was added NaH (11.6 mmol). Note: excess NaH was added due to excess tButyl ethyl malonate carried over from 2a. The solution was agitated for 10 minutes. A solution of 2a/2b/malonate (5.15 mmol, corrected for assay) in THF (20 mL) was rapidly added to the first solution. The resulting solution was agitated at 30° C. for 18 hours, then at 55° C. for 2 hours. After allowing to cool to room temperature, the solution was quenched with water (400 μL), dried over Na2SO4 and concentrated in vacuo yielding a yellow oil which was purified by flash chromatography (silica, Gradient system: 1. Ethyl acetate, 2. 10% Methanol in Ethyl acetate). Upon concentration a yellow oil 3 (1.096 g, 45.2% yield) with an isomeric ratio of 3.3:1 was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07626031B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-59ad08d340024a5faa8c764f8c6a6053 |
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| Source note | uspto-grants-2009_12 |
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