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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5293Erstellt: 24. Oktober 2026

1-Naphthol → 2-Bromo-1-methoxynaphthalene

https://huagongshe.com/de/reaction/5293

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-NaphtholHCID 7005—
EduktPotassium CarbonateHCID 11430—
Edukt2-Bromo-1-naphtholHCID 150849—
EduktN-bromo-t-butylamineHCID 11789384—
LösungsmittelAcetoneHCID 180—
Produkt2-Bromo-1-methoxynaphthaleneHCID 12612830—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

1-naphthol was converted into 2-bromo-1-naphthol by reaction with a slurry of N-bromo-t-butylamine at -78° C. according to the procedure described in Pearson, Wysong, Breder, J. Org. Chem. 32, 2358 (1967). To a solution of 1 mole (crude) of the bromonaphthol in 750 mL of acetone was added 175 g of potassium carbonate. Over a 2-hous period, 95 mL of dimethylsulate was added dropwise to the mechanically stirred reaction mixture. The resulting slurry was stirred at 25° C. overnight. The solids were filtered and the solution was stripped to yield a dark brown oil. Initial purification was accomplished by vacuum distillation (80°-120° C., 0.2 Torr) followed by further purification by HPLC with hexane to yield 145 g of 2-bromo-1-methoxynaphthalene as a pale yellow oil. NMR confirmed the structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244771
Quelldatensatzuspto-grants-1993_09
ORD IDord-352027f5ace04caca5d1f5c9a25194cf
Quellennotizuspto-grants-1993_09