HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2247846Erstellt: 25. Oktober 2026
Epichlorohydrin → 1-Benzyloxy-4-(2,3-epoxypropyl)-naphthyl ether
https://huagongshe.com/reaction/2247846
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Epichlorohydrin | HCID 7835 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-(Benzyloxy)naphthalen-1-ol | HCID 562937 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-Benzyloxy-4-(2,3-epoxypropyl)-naphthyl ether | HCID 57266200 | — |
Reaktionsschritte
To a solution of 4.3 g. (0.017 mole) 1-hydroxy-4-benzyloxynaphthalene in 15 ml. (0.19 mole) epichlorohydrin, which is heated to its boiling point while stirring, is carefully added dropwise 3.7 ml. 5M aqueous sodium hydroxide solution (0.0187 mole). The apparatus used for carrying out the reaction is equipped with a water separator so that the water distils off azeotropically from the reaction mixture with epichlorohydrin. After distilling off the theoretical amount of water, the reaction mixture is further heated under reflux for 1 hour while stirring, thereafter mixed with 50 ml. toluene, filtered off from inorganic components and the solution evaporated on a rotary evaporator. The product obtained is used for the next reaction step without further purification. Yield 6.1 g.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05037828 |
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| Quelldatensatz | uspto-grants-1991_08 |
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| ORD ID | ord-a7db72b6b20d4e5e8c4103c466e52550 |
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| Quellennotiz | uspto-grants-1991_08 |
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