戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 969475作成日:2026年10月26日

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

https://huagongshe.com/reaction/969475

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Sodium hydrideHCID 24758—
反応物1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
反応物Methyl 6-hydroxy-2-naphthoateHCID 390995—
溶媒DimethylformamideHCID 6228—
生成物Methyl 6-(2-methoxyethoxymethoxy)naphthalene-2-carboxylateHCID 1208548485%

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07307078B2
出典データセットuspto-grants-2007_12
ORD IDord-46d1260935e44f699670d3851c25d14e
出典メモuspto-grants-2007_12