참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4,6-Dimethyl-2-methylsulfonylpyrimidine | HCID 2772382 | — |
| 반응물 | Methyl 2-hydroxy-3,3-dimethylbutanoate | HCID 9855510 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Methyl 2-(4,6-dimethylpyrimidin-2-yl)oxy3,3-dimethylbutyrate | HCID 15070275 | 83.9% |
반응 단계
2.9 g of methyl 2-hydroxy-3,3-dimethybutyrate, 4.1 g of 4,6 -dimethyl-2-methylsulfonylpyrimidine and 3.3 g of potassium carbonate were added to 50 ml of N,N-dimethylformamide, and the mixture was stirred at 100° C. for 4 hours. The reaction solution was cooled to room temperature, poured into water and extracted with 100 ml of ethyl acetate. The organic layer was washed twice with a sodium chloride aqueous solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The liquid substance thereby obtained was purified by silica gel column chromatography (eluent: hexane/ethyl acetate =6/1) to obtain 4.2 g of the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04968340 |
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| 출처 데이터셋 | uspto-grants-1990_11 |
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| ORD ID | ord-93c1f599379a44d6846451f41d515ed7 |
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| 출처 메모 | uspto-grants-1990_11 |
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