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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357482생성일: 2026년 10월 25일

Potassium Carbonate → Methyl (+/-)-2-(4,6-dimethoxy-2-pyrimidinyloxy)-3,3-dimethylbutanoate

https://huagongshe.com/reaction/357482

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Methyl 2-hydroxy-3,3-dimethylbutanoateHCID 9855510—
반응물4,6-Dimethoxy-2-methyl-sulfonylpyrimidineHCID 77134791—
용매DimethylformamideHCID 6228—
생성물Methyl (+/-)-2-(4,6-dimethoxy-2-pyrimidinyloxy)-3,3-dimethylbutanoateHCID 11011508—

반응 단계

2.18 g (10.0 mmol) of 4,6-dimethoxy-2-methyl-sulfonylpyrimidine and 1.62 g (11.0 mmol) of methyl (+/-)-2-hydroxy-3,3-dimethylbutanoate were heated in the presence of 2.07 g (15.0 mmol) of potassium carbonate in 20 ml of N,N-dimethylformamide to 60° with stirring. After 3 hours, the solvent was removed in a rotary evaporator at 60° C./20 mbar. The residue was taken up in 40 ml of water and 40 ml of ethyl acetate. After the organic phase had been separated off, the aqueous phase was again extracted with 40 ml of ethyl acetate. The combined organic phases was washed with water, dried over magnesium sulfate and evaporated. The title product was obtained in a yield of 2.76 g (93.8 percent of theory) in the form of pale yellowish crystals (GC content 96.6 percent).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840892
출처 데이터셋uspto-grants-1998_11
ORD IDord-adbef3802671476d8d696eb6b9720bf6
출처 메모uspto-grants-1998_11