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HRID 2274189作成日:2026年10月27日

Diethyl Oxalate → Ethyl (3,5-dimethoxyphenyl)(oxo)acetate

https://huagongshe.com/reaction/2274189

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl OxalateHCID 7268—
反応物1-Bromo-3,5-dimethoxybenzeneHCID 639187—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl (3,5-dimethoxyphenyl)(oxo)acetateHCID 2472225671.4%

反応条件

温度-78 °C

反応手順

To a solution of 1-bromo-3,5-dimethoxybenzene (2.17 g, 10 mmol) in THF (15 mL) was dropwise added n-butyl lithium (8 mL, 2.5 mol/L in hexane, 20 mmol) at −78° C. After stirring for 50 mins at −78° C. a solution of diethyl oxalate (4 g, 27 mmol) in THF (10 mL) was added. The mixture was stirred at −78° C. for another 4 h, then quenched with saturated ammonium chloride and extracted with ethyl acetate (50 mL*3). The organic layers were combined, washed by brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by chromatography on silica gel to give the title compound (1.7 g, 71%). MS (ES+) C12H14O5 requires: 238. Found: 239 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09126951B2
出典データセットuspto-grants-2015_09
ORD IDord-0b4ad86dcbad4bd3b7fe89d5ad50c25d
出典メモuspto-grants-2015_09