HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 606156Erstellt: 25. Oktober 2026
Water → 2-(1-Benzylpiperidin-4-yl)-1-(2-chlorophenyl)ethanol
https://huagongshe.com/reaction/606156
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 1-Bromo-2-chlorobenzene | HCID 12754 | — |
| Edukt | 4-Piperidineacetaldehyde, 1-(phenylmethyl)- | HCID 10013602 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-(1-Benzylpiperidin-4-yl)-1-(2-chlorophenyl)ethanol | HCID 22248584 | — |
Reaktionsschritte
After dissolving 1.75 ml of 1-bromo-2-chlorobenzene in 30 ml of tetrahydrofuran, the solution was cooled to −78° C. Next, 5.31 ml of n-butyllithium (2.6 M, n-hexane solution) was added dropwise thereto while stirring and after 1 hour, a solution of 2.50 g of 1-benzylpiperidine-4-acetaldehyde in tetrahydrofuran (10 ml) was added and stirring was continued for 1 hour. After adding water to the reaction solution, the temperature was raised to room temperature and extraction was performed with ethyl acetate. The organic layer was washed with water and saturated brine in that order and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure to obtain 2-(1-benzylpiperidin-4-yl)-1-(2-chlorophenyl)ethanol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07915274B2 |
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| Quelldatensatz | uspto-grants-2011_03 |
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| ORD ID | ord-08da84c0378748d1ad2defc78b07a4fd |
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| Quellennotiz | uspto-grants-2011_03 |
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