Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2231467생성일: 2026년 10월 27일
Potassium Carbonate → 4-[4-Acetyl-3-[2-[2-[(methylsulfonyl)oxy]ethoxy]-ethoxy]-2-propylphenoxy]butanoic acid ethyl ester
https://huagongshe.com/reaction/2231467
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Diethylene Glycol Dimethanesulfonate | HCID 147571 | — |
| 반응물 | Ethyl 4-(4-acetyl-3-hydroxy-2-propylphenoxy)butanoate | HCID 14330004 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-[4-Acetyl-3-[2-[2-[(methylsulfonyl)oxy]ethoxy]-ethoxy]-2-propylphenoxy]butanoic acid ethyl ester | HCID 14330009 | 67% |
반응 단계
A mixture of 4 g (0.013 mol) of 4-(4-acetyl-3-hydroxy-2-propylphenoxy)butanoic acid ethyl ester, 17 g (0.065 mol) of diethylene glycol dimesylate and 3.6 g (0.026 mol) of anhydrous potassium carbonate in 80 ml of anhydrous acetone and 40 ml of anhydrous dimethylformamide was stirred at reflux for 20 hours. An additional 1.8 g of potassium carbonate was added and reflux was continued for a total of 44 hours. The reaction mixture was filtered and concentrated in vacuo to an orange oil which was treated with ethyl acetate and sodium chloride solution. The yellow oil obtained on concentration of the ethyl acetate was purified by HPLC, eluting with 15% ethyl acetate/toluene to yield 4.1 g (67% yield) of 4-[4-acetyl-3-[2-[2-[(methylsulfonyl)oxy]ethoxy]-ethoxy]-2-propylphenoxy]butanoic acid ethyl ester as a yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04782176 |
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| 출처 데이터셋 | uspto-grants-1988_11 |
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| ORD ID | ord-0323c499dec241fcbe0cc5d56c29bdf8 |
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| 출처 메모 | uspto-grants-1988_11 |
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