HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 423543Erstellt: 25. Oktober 2026
Diethyl Ether → {1-[3-(1-Methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanol
https://huagongshe.com/reaction/423543
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 4-(Hydroxymethyl)piperidine-1-carbonitrile | HCID 51358289 | — |
| Edukt | HCID 178449908 | HCID 178449908 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | {1-[3-(1-Methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanol | HCID 57930076 | 438% |
Reaktionsschritte
A solution of 1N ZnCl2 in Et2O (182 mL, 182 mmol) was added to a solution of 4-(hydroxymethyl)-1-piperidinecarbonitrile (21.3 g, 152 mmol) and N-hydroxy-2-methylpropanimidamide (18.6 g, 182 mmol) in EtOAc (50 mL) at ambient temperature. The reaction mixture was left at ambient temperature for 30 min, decanted, and was treated with concentrated HCl (45 mL) and ethanol 20 mL). The mixture was heated at reflux for 2 h. The mixture was evaporated to dryness, and the resulting residue was charged with water and the pH was adjusted to basic with K2CO3. The mixture was extracted with EtOAc and the material obtained was combined with 9 other batches prepared similarly and purified by silica gel chromatography to give 150 g of {1-[3-(1-methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08101634B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-132c494bbfdd4826bd3d9099cd03ce51 |
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| Quellennotiz | uspto-grants-2012_01 |
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