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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1375139Erstellt: 26. Oktober 2026

Ethyl chloroformate → Ethyl 1,4-dimethoxy-3-methyl-2-naphthoate

https://huagongshe.com/reaction/1375139

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl chloroformateHCID 10928—
Edukt2-Bromo-1,4-dimethoxy-3-methylnaphthaleneHCID 292240—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 1,4-dimethoxy-3-methyl-2-naphthoateHCID 1136935289%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

n-Butyl lithium (1.6M in hexanes, 4.1 ml, 6.56 mmol) was added dropwise to 2-bromo-1,4-dimethoxy-3-methylnaphthalene (1.537 g, 5.47 mmol) in tetrahydrofuran (30 ml) at −50° C. The reaction was stirred for 30 min at −50° C. before dropwise addition of ethyl chloroformate (1 ml, 10.46 mmol). The reaction was allowed to warm to 0° C. over 18 h quenched by addition of hydrochloric acid (2N) and extracted with ethyl acetate. The extract was dried (Na2SO4) and the solvent evaporated under vacuum. The residue was purified by SPE (silica, 10 g) eluting with 10% ethyl acetate in cyclohexane to give ethyl 1,4-dimethoxy-2-methylnaphthalene-3-carboxylate (1.33 g, 89%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07166631B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-58c8d308fd31452db0c1522c0c54ce8d
Quellennotizuspto-grants-2007_01