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HRID 15718Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/15718

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
PatentnummerUS07732622B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-68ac42a1003a457896b8b3eb493ce566
Quellennotizuspto-grants-2010_06