HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1168948Erstellt: 26. Oktober 2026
Sodium Chloride → 5-(3-Chloropropoxy)-3-(phenylmethoxy)pyridine
https://huagongshe.com/reaction/1168948
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 1-Chloro-3-iodopropane | HCID 81363 | — |
| Edukt | 3-Benzyloxy-5-hydroxypyridine | HCID 22989704 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 5-(3-Chloropropoxy)-3-(phenylmethoxy)pyridine | HCID 22989698 | — |
Reaktionsschritte
Under a nitrogen atmosphere, a solution of 5-(phenylmethoxy)pyridine-3-ol (1.52 g, 7.56 mmol) in N,N-dimethylformamide (DMF) (10 mL) was added drop-wise over 5 min to a cold (0-5° C.), stirring slurry of sodium hydride (0.238 g of an 80% dispersion in mineral oil, 7.94 mmol) in DMF (15 mL). The mixture was allowed to stir and warm to ambient temperature over 1 h. Next, 1-chloro-3-iodopropane (1.85 g, 9.07 mmol) was added drop-wise over 5 min. The resulting dark-brown mixture was stirred at ambient temperature for 4 h. Water (25 mL) was added, followed by saturated NaCl solution (25 mL), and the mixture was extracted with ether (4×50 mL). The combined ether extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06627648B1 |
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| Quelldatensatz | uspto-grants-2003_09 |
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| ORD ID | ord-87e927aeec304c8a91c4153a1559cab3 |
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| Quellennotiz | uspto-grants-2003_09 |
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