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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31354생성일: 2026년 10월 24일

Diethyl Oxalate → Ethyl 2-methoxybenzoylformate

https://huagongshe.com/ko/reaction/31354

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl OxalateHCID 7268—
반응물2-BromoanisoleHCID 11358—
반응물Ammonium ChlorideHCID 25517—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매PentaneHCID 8003—
생성물Ethyl 2-methoxybenzoylformateHCID 15579652—

반응 단계

A solution of 27 g of 1-bromo-2-methoxybenzene in 270 ml of ether is cooled to −70° C. under an argon atmosphere, 90 ml of a 1.6 M solution of n-butyl-lithium in pentane are added dropwise and the mixture is then left stirring for 45 minutes. 78 ml of diethyl oxalate are added rapidly and the mixture is left stirring, while allowing the temperature to return to RT. After stirring for 1 hour at RT, saturated NH4Cl solution is added to the mixture, the phases are separated after settling has taken place, the aqueous phase is extracted with ether, the combined organic phases are washed with water and then with saturated NaCl solution and dried over Na2SO4, and the solvents are evaporated off under vacuum. The excess diethyl oxalate is removed by distillation under vacuum (b.p.=87° C. at 2 000 Pa). The resulting product is chromatographed on silica gel, eluting with a DCM/hexane mixture (50/50; v/v) and then with DCM. The product obtained is purified by distillation under vacuum. 13 g of the expected product are obtained; b.p.=110° C. at 3 Pa.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425566B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-e1496e4568d7464da8f731298c452447
출처 메모uspto-grants-2008_09