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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Methyl 2-hydroxy-3,3-dimethylbutanoate | HCID 9855510 | — |
| 반응물 | 4,6-Dimethoxy-2-methyl-sulfonylpyrimidine | HCID 77134791 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Methyl (+/-)-2-(4,6-dimethoxy-2-pyrimidinyloxy)-3,3-dimethylbutanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05840892 |
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| 출처 데이터셋 | uspto-grants-1998_11 |
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| ORD ID | ord-adbef3802671476d8d696eb6b9720bf6 |
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| 출처 메모 | uspto-grants-1998_11 |
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