HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 60806Erstellt: 24. Oktober 2026
Triethylamine → 2-(6-Methylpyridin-2-yl)ethyl methanesulfonate
https://huagongshe.com/de/reaction/60806
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | 6-Methylpyridine-2-ethanol | HCID 70283 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-(6-Methylpyridin-2-yl)ethyl methanesulfonate | HCID 87885158 | — |
Reaktionsschritte
MsCl (6.7 mmol, 0.52 mL) was added to a solution of 6-methyl-2-pyridineethanol (6.7 mmol, 0.92 g) and triethyl amine (13.4 mmol, 1.88 mL) in toluene (6 mL) at 0° C. dropwise. The resulting mixture was stirred at 0° C. for 30 min. The precipitate generated from reaction was filtered off. The filtrate was concentrated in vacuo to give crude 2-(6-methylpyridin-2-yl)ethyl methanesulfonate which was used for next step without further purification. A mixture of above described 2-(6-methylpyridin-2-yl)ethyl methanesulfonate, PhOH (13.4 mmol, 1.26 g) and NaOH (13.4 mmol, 0.54 g) in isopropanol (20 mL) was refluxed at 90° C. for 3 h. The reaction mixture was concentrated in vacuo and dissolved in EtOAc which was washed with water. The organic layer was separated, dried with MgSO4 and concentrated in vacuo. The crude product was purified by chromatography to give desired 2-methyl-6-(2-phenoxyethyl)pyridine as a colorless oil in 26% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09440982B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-5815eb26c1a244d6995a88f54424a4fe |
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| Quellennotiz | uspto-grants-2016_09 |
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