돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1930123생성일: 2026년 10월 26일

Diethyl Malonate → Diethyl 2-(2,5-dichloro-4-methoxyphenyl)malonate

https://huagongshe.com/reaction/1930123

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl MalonateHCID 7761—
반응물Cesium carbonateHCID 10796—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물1-Bromo-2,5-dichloro-4-methoxybenzeneHCID 59627679—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
생성물Diethyl 2-(2,5-dichloro-4-methoxyphenyl)malonateHCID 5962772837.6%

반응 조건

온도100 °C

반응 단계

A solution of 1-bromo-2,5-dichloro-4-methoxybenzene (Intermediate 4-6; 3.82 g, 14.93 mmol), cesium carbonate (14.59 g, 44.78 mmol) and dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (0.427 g, 0.90 mmol) in toluene (220 mL) was thoughroughly degassed. The mixture was treated with diacetoxypalladium (0.101 g, 0.45 mmol) and diethyl malonate (2.505 mL, 16.42 mmol) and the resulting solution stirred under a nitrogen atmosphere at 100° C. for 18 hours. The reaction mixture was allowed to cool to ambient temperature, evaporated to dryness and partitioned between EtOAc (150 mL) and water (100 mL). The mixture was filtered and the aqueous layer was separated and re extracted with EtOAc (150 mL). The organic extracts were combined, dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford diethyl 2-(2,5-dichloro-4-methoxyphenyl)malonate (1.880 g, 37.6%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08188092B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-0d585eff1bc74209b30b86a66cc1c17c
출처 메모uspto-grants-2012_05