HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352407Generated: October 26, 2026
Ethylenediamine → (Z)-7-[2-Oxo-6-((E)-3-oxo-oct-1-enyl)-piperidin-1-yl]-hept-5-enoic acid methyl ester
https://huagongshe.com/reaction/352407
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 7-[2-Oxo-6-((E)-3-oxo-oct-1-enyl)-piperidin-1-yl]-hept-5-ynoic acid methyl ester | HCID 10406302 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel Dichloride | HCID 24385 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (Z)-7-[2-Oxo-6-((E)-3-oxo-oct-1-enyl)-piperidin-1-yl]-hept-5-enoic acid methyl ester | HCID 11726242 | 43% |
Reaction Steps
A 50 mL round bottom flask was charged with nickel (II) chloride (273 mg, 2.10 mmol) and sodium borohydride (40 mg, 1.05 mmol), then 95% ethanol (2.0 mL) was added. The mixture immediately turned black. After 15 min at rt, ethylene diamine (0.23 mL, 3.36 mmol) was added. After another 15 min at rt, 7-[2-oxo-6-((E)-3-oxo-oct-1-enyl)-piperidin-1-yl]-hept-5-ynoic acid methyl ester (152 mg, 0.42 mmol) in 95% ethanol (2.0 mL) was added via cannula. A hydrogen atmosphere was established by evacuating and refilling with hydrogen (3×) and the reaction mixture was stirred under a balloon of hydrogen for 19 h. The reaction mixture was filtered through celite, washing with ethanol, and the filtrate was concentrated in vacuo. Purification of the resulting residue by flash column chromatography (10→50% EtOAc/CH2Cl2, gradient) afforded 65 mg (43%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06747037B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-caa38115556a4f0c8a6757532b890432 |
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| Source note | uspto-grants-2004_06 |
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