HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 911436Erstellt: 25. Oktober 2026
Triethylamine → (R)-Methanesulfonic acid 1-(6-methyl-pyridin-2-yl)-ethyl ester
https://huagongshe.com/reaction/911436
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | (R)-1-(6-methylpyridin-2-yl)ethanol | HCID 45079484 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (R)-Methanesulfonic acid 1-(6-methyl-pyridin-2-yl)-ethyl ester | HCID 57656393 | 100% |
Reaktionsschritte
To a stirred solution of (R)-1-(6-methyl-pyridin-2-yl)-ethanol (175 mg, 1.28 mmol) and triethylamine (355 μl, 2.56 mmol) in DCM (5 mL) at 0° C. add methanesulfonyl chloride (148 μl, 1.92 mmol). Stir at 0° C. for 30 min and quench the reaction mixture with saturated aqueous NaHCO3 at the same temperature. Extract the mixture three times with EtOAc, dry over anhydrous Na2SO4, and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane/EtOAc (8:2) to give the title compound as a colorless oil (274 mg, 100%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08022062B2 |
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| Quelldatensatz | uspto-grants-2011_09 |
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| ORD ID | ord-6032a6bb22f94cbebbbcac7c892c9f96 |
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| Quellennotiz | uspto-grants-2011_09 |
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