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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2253571생성일: 2026년 10월 25일

Dimethylformamide → Ethyl 2-(4,6-dimethylpyrimidin-2-yl)oxyacetate

https://huagongshe.com/reaction/2253571

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물Ethyl GlycolateHCID 12184—
반응물4,6-Dimethyl-2-methylsulfonylpyrimidineHCID 2772382—
용매WaterHCID 962—
생성물Ethyl 2-(4,6-dimethylpyrimidin-2-yl)oxyacetateHCID 3410252—

반응 단계

A solution containing 4,6-dimethyl-2-methylsulfonylpyrimidine (10.0 g, 53.8 mmol), ethyl glycolate (5.60 g, 53.8 mmol), and 30 mL of N,N-dimethylformamide was prepared and to this was added with stirring potassium carbonate (8.0 g, 60 mmol). The mixture was allowed to stir at ambient temperature overnight. It was then poured into water and the resulting mixture was extracted 3 times with ethyl acetate. The combined organic extracts were extracted with water. The aqueous extract was saturated with sodium chloride and extracted twice more with ethyl acetate. All of the ethyl acetate layers were combined, dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain 8.20 g (72.6 percent of theory) of the title compound as a yellow oil. This oil was filtration chromatographed on silica gel, eluting with a 30:70 mixture of ethyl acetate and hexane. The product containing eluate was concentrated by evaporation under reduced pressure to obtain 7.9 g (70 percent of theory) of the title compound as a colorless oil which solidified on standing to a white solid melting at 57°-59° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05232896
출처 데이터셋uspto-grants-1993_08
ORD IDord-079c33fee04d497294ff221bd8620f79
출처 메모uspto-grants-1993_08