Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221849생성일: 2026년 10월 24일
1-(4-Methoxyphenyl)butane-1,3-dione → 4-(4-Methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl ester
https://huagongshe.com/ko/reaction/221849
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-(4-Methoxyphenyl)butane-1,3-dione | HCID 77640 | — |
| 반응물 | Sodium ethoxide | HCID 2723922 | — |
| 반응물 | Ethyl chloro(hydroximino)acetate | HCID 6816376 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 4-(4-Methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl ester | HCID 59652027 | — |
반응 단계
To 7.04 mL of 21% sodium ethoxide in ethanol (18.8 mmol) in 60 mL ethanol at 0° C. was added 4.70 g of 1-(4-methoxyphenyl)butane-1,3-dione (17.1 mmol) in 60 mL ethanol dropwise over 24 minutes. After 30 min a solution of 2.59 g of ethyl chloro-(hydroximino)acetate (17.1 mmol) in 30 mL ethanol was added dropwise over 6 minutes. The reaction was warmed to room temperature slowly. When TLC indicated the reaction was complete, the reaction was concentrated in vacuo. Water and saturated NaHCO3 was added and the product extracted with ethyl acetate. The ethyl acetate extracts were dried with Na2SO4, filtered, and concentrated in vacuo. The crude material was purified via silica gel chromatography eluting with 8:1 hexane:ethyl acetate to give 4-(4-methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl ester which was dried overnight under high vacuum to give 3.74 g (71.8%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08207168B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-61dc1495a4384999961add7a19d8179b |
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| 출처 메모 | uspto-grants-2012_06 |
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