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HRID 15718作成日:2026年10月25日

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

https://huagongshe.com/reaction/15718

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl chloroformateHCID 10928—
反応物2-Bromo-1,4-dimethoxy-3-methylnaphthaleneHCID 292240—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 1,4-dimethoxy-3-methyl-2-naphthoateHCID 1136935289%

反応条件

温度0 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732622B2
出典データセットuspto-grants-2010_06
ORD IDord-68ac42a1003a457896b8b3eb493ce566
出典メモuspto-grants-2010_06