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HRID 31346생성일: 2026년 10월 23일

Veratrole → Ethyl 2-(2,3-dimethoxyphenyl)-2-oxoacetate

https://huagongshe.com/ko/reaction/31346

반응식

참여 물질

역할이름HCID투입량
반응물VeratroleHCID 7043—
반응물Diethyl OxalateHCID 7268—
반응물Ammonium ChlorideHCID 25517—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물Ethyl 2-(2,3-dimethoxyphenyl)-2-oxoacetateHCID 21905960—

반응 조건

온도-40 °C

반응 단계

A mixture of 27.6 g of 1,2-dimethoxybenzene in 160 ml of ether is cooled to −40° C., 250 ml of a 1.6 M solution of n-butyllithium in hexane are added dropwise and the mixture is then left stirring for 24 hours while allowing the temperature to return to RT. The reaction mixture is cooled to −20° C., 136 ml of diethyl oxalate are added rapidly and the mixture is left stirring while allowing the temperature to return to RT. After stirring for 30 minutes at RT, the reaction mixture is poured into saturated NH4Cl solution, the phases are separated after settling has taken place, the aqueous phase is extracted with ether, the combined organic phases are washed twice with water and dried over Na2SO4, and the solvents are evaporated off under vacuum. The excess diethyl oxalate is removed by distillation under vacuum (b.p.=90° C. at 2 400 Pa). The resulting crude product is chromatographed on silica gel, eluting with a heptane/iso ether mixture (90/10; v/v). 25 g of the expected product are obtained and are used without further purification in the following step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425566B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-87833b48f9224b76829b3ae1464e07ed
출처 메모uspto-grants-2008_09