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HRID 455563作成日:2026年10月26日

Diethyl Oxalate → Ethyl 2-(5-bromo-2-(methoxymethoxy)phenyl)-2-oxoacetate

https://huagongshe.com/reaction/455563

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2,4-Dibromo-1-(methoxymethoxy)benzeneHCID 10565833—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物Ethyl 2-(5-bromo-2-(methoxymethoxy)phenyl)-2-oxoacetateHCID 57475646112.8%

反応手順

A solution of 2,4-dibromo-1-(methoxymethoxy)benzene (40.5 g, 137 mmol) in Et2O (140 mL) was cooled to −78° C. and treated with n-BuLi (2.5M in hexanes; 60.2 mL, 151 mmol) under nitrogen atmosphere. After 30 minutes a solution of diethyl oxalate (27.9 mL, 205 mmol) in Et2O (20 mL) was added dropwise. The reaction mixture was stirred for 45 minutes at that temperature then quenched cold with saturated ammonium chloride solution. The mixture was partitioned between Et2O and water. The organic phase was separated, washed with water, brine, then dried over MgSO4. The solvent was removed under reduced pressure to afford 49 g of ethyl 2-(5-bromo-2-(methoxymethoxy)phenyl)-2-oxoacetate, which was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08497264B2
出典データセットuspto-grants-2013_07
ORD IDord-c8a2fe41913f4aea80c8466dc2776192
出典メモuspto-grants-2013_07