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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1618Erstellt: 24. Oktober 2026

Propargyl bromide → Methyl-3-propargyloxy-2-naphthoate

https://huagongshe.com/de/reaction/1618

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropargyl bromideHCID 7842—
EduktSodium hydrideHCID 24758—
EduktMethyl 3-hydroxy-2-naphthoateHCID 70163—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl-3-propargyloxy-2-naphthoateHCID 5426244635%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726187
Quelldatensatzuspto-grants-1998_03
ORD IDord-33fdd502bd9b4b6ab4abded4f14a5ab2
Quellennotizuspto-grants-1998_03