HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1618Erstellt: 24. Oktober 2026
Propargyl bromide → Methyl-3-propargyloxy-2-naphthoate
https://huagongshe.com/de/reaction/1618
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Propargyl bromide | HCID 7842 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Methyl 3-hydroxy-2-naphthoate | HCID 70163 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Methyl-3-propargyloxy-2-naphthoate | HCID 54262446 | 35% |
Reaktionsschritte
Methyl-3-hydroxy-2-naphthoate (2.63 g, 0.013 mol) was dissolved in dry THF (80 ml) and treated with sodium hydride (80%) ((0.398 g, 0.013 mol), with stirring under N2. After 0.5 h, propargyl bromide (80% in toluene) (2.57 ml 0.017 mol) was added and the mixture heated to reflux. After 20 h, the reaction mixture was allowed to cool and then evaporated under reduced pressure. The residue was then evaporated under reduced pressure. The residue was then partitioned between EtOAc and water. The aqueous layer was then extracted with EtOAc (1×), and the combined organic layers were dried (Na2SO4) and evaporated to given an orange oil. Crystallisation of the oil from petrol (60/80) diethyl ether provided the title compound as a pale yellow solid (1.0 gg, 35%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05726187 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-33fdd502bd9b4b6ab4abded4f14a5ab2 |
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| Quellennotiz | uspto-grants-1998_03 |
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