Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 719181Erstellt: 26. Oktober 2026

Methyl iodide → 8-Amino-2-naphthalenol

https://huagongshe.com/reaction/719181

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukt8-Amino-2-naphthalenolHCID 8358—
EduktCleve's acidHCID 8386—
EduktSodium hydrideHCID 24758—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt8-Amino-2-naphthalenolHCID 8358—
Produkt7-Methoxynaphthalen-1-amineHCID 235817—

Reaktionsschritte

8-Amino-naphthalen-2-ol was prepared from 8-amino-2-naphthalenesulphonic acid (commercially available) according to the literature (J. Org. Chem. 1949, p351). To a solution of 8-amino-naphthalen-2-ol (8.00 g) in dry N,N-dimethylformamide (80 mL) was added sodium hydride (60% dispersion in mineral oil, 3.2 g) carefully. After stirring for 4 hours the reaction mixture was cooled in an ice bath and methyl iodide (3.13 mL) was added dropwise. The reaction mixture was then stirred at room temperature for 3 days. Water (10 mL) was then added and the volatiles were removed in vacuo. The residue was dissolved in chloroform, washed with water, dried (MgSO4) and the solvent removed in vacuo to yield a dark oil. This was purified using flash chromatography (chloroform) to yield 7-methoxy-naphthalen-1-ylamine as a dark brown liquid (2.92 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07132419B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-d39c13159e5342e598803700f91173f1
Quellennotizuspto-grants-2006_11