HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1471724Erstellt: 25. Oktober 2026
Chloromethyl Methyl Ether → 2-(Benzyloxy)-5-(methoxymethoxy)pyridine
https://huagongshe.com/reaction/1471724
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloromethyl Methyl Ether | HCID 7864 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 6-(Benzyloxy)pyridin-3-ol | HCID 42553041 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-(Benzyloxy)-5-(methoxymethoxy)pyridine | HCID 67217684 | 87% |
Reaktionsschritte
To a solution of 6-(benzyloxy)pyridin-3-ol (2.0 g, 10 mmol, 1 eq.) in DMF (20 mL) was added NaH (60% in mineral oil; 0.6 g, 15 mmol, 1.5 eq.) at 0-5° C. portion-wise. Upon the completion of addition, the mixture was continued to stir at 0-5° C. for 15 min, added chloromethyl methyl ether (0.88 g, 11 mmol, 1.1 eq.), stirred at 0-5° C. for another 20 min, and quenched with NH4Cl(sat) solution. The aqueous layer was extracted with EtOAc (3×20 mL) and the combined organic layers were washed with water and brine, dried over Na2SO4, concentrated, and purified on silica gel using 25% EtOAc/hexanes as eluent to give 2-(benzyloxy)-5-(methoxymethoxy)pyridine (2.1 g, 87%) as a colorless oil. LRMS (M+H+) m/z 246.1
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09012450B2 |
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| Quelldatensatz | uspto-grants-2015_04 |
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| ORD ID | ord-01ca7b649ba94b27a94818f00f276560 |
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| Quellennotiz | uspto-grants-2015_04 |
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