HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 606154Erstellt: 24. Oktober 2026
Dimethyl Sulfoxide → 1-(1-Benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanone
https://huagongshe.com/de/reaction/606154
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | 1-(1-Benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanol | HCID 22248173 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-(1-Benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanone | HCID 22247993 | 73% |
Reaktionsschritte
After dissolving 7.5 ml of oxalyl chloride in 130 ml of dichloromethane, the solution was cooled to −78° C. and a solution of 6.1 ml of dimethylsulfoxide in dichloromethane (20 ml) was added dropwise while stirring. After stirring for 20 minutes, a solution of 13.4 g of 1-(1-benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanol in dichloromethane (40 ml) was added dropwise. After stirring for 30 minutes, 24 ml of triethylamine was added and the temperature was raised to room temperature. Water was added to the reaction solution, 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. The residue was purified by NH silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (9.64 g, 73% yield).
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-722ea4779f1247ca9b73bbff3e9331fa |
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| Quellennotiz | uspto-grants-2011_03 |
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