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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 563453Erstellt: 23. Oktober 2026

Dimethyl Sulfoxide → 1-Bromo-2-methoxynaphthalene

https://huagongshe.com/de/reaction/563453

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktMethyl iodideHCID 6328—
Edukt1-Bromo-2-naphtholHCID 11316—
EduktPotassium HydroxideHCID 14797—
LösungsmittelWaterHCID 962—
Produkt1-Bromo-2-methoxynaphthaleneHCID 7286069%

Reaktionsschritte

A 500 mL three-necked round-bottomed flask was charged with 1-bromonaphthalen-2-ol (30.0 g, 134.5 mmol), potassium hydroxide (KOH) (11.3 g, 201.7 mmol) and DMSO (300 mL), and the mixture was stirred under nitrogen atmosphere for 10 minutes, After cooling the mixture by using ice-water bath, iodomethane (28.6 g, 201.7 mmol) was slowly added dropwise thereto. Then, the resultant mixture was stirred under nitrogen atmosphere at ambient temperature for 12 hours, and then at 50° C. for 1 hour. After cooling to ambient temperature, the reaction mixture was mixed with water (500 mL), and extracted with diethyl ether. Organic mixture was washed three times with distilled water, and dried over anhydrous magnesium sulfate (MgSO4). After removing the solvent by using a rotary evaporator, the residue was purified via silica gel column chromatography (eluent: n-hexane) to obtain 1-bromo-2-methoxynaphthalene (22.0 g, yield: 69.0%) as white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08067511B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-5f3bba70d52444a189792b56345d99b6
Quellennotizuspto-grants-2011_11