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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 969475Erstellt: 24. Oktober 2026

Tetrahydrofuran → Methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate

https://huagongshe.com/de/reaction/969475

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktSodium hydrideHCID 24758—
Edukt1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
EduktMethyl 6-hydroxy-2-naphthoateHCID 390995—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylateHCID 1208548485%

Reaktionsschritte

3.3 g (83 mmol) of 60% sodium hydride in oil are added portionwise to a solution of 14 g (69 mmol) of methyl 6-hydroxynaphthalene-2-carboxylate in 180 ml of an equivolume mixture of tetrahydrofuran and dimethylformamide. After the evolution of gas has ceased, 8.7 ml (76 mmol) of methoxyethoxymethyl chloride are added dropwise. The reaction medium is stirred at room temperature for 3 hours, immersed into ice-cold water and extracted with ethyl ether. The organic phase is dried over sodium sulfate, filtered and concentrated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture. 17 g of methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylate are obtained in the form of a colorless oil, in a yield of 85%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07307078B2
Quelldatensatzuspto-grants-2007_12
ORD IDord-46d1260935e44f699670d3851c25d14e
Quellennotizuspto-grants-2007_12