Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2221642생성일: 2026년 10월 26일
2-Oxime 2,3-butanedione → Ethyl 5-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)thiophene-2-carboxylate
https://huagongshe.com/reaction/2221642
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Oxime 2,3-butanedione | HCID 6398969 | — |
| 반응물 | Ethyl 5-formylthiophene-2-carboxylate | HCID 10797570 | — |
| 반응물 | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| 생성물 | Ethyl 5-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)thiophene-2-carboxylate | HCID 23076614 | 24% |
반응 단계
A mixture of ethyl 5-formylthiophene-2-carboxylate (14.6 g), 2,3-butanedione-2-oxime (8.02 g) and 4N hydrogenchloride-ethyl acetate (300 mL) was stirred at room temperature for 15 hrs. The reaction mixture was concentrated, diethyl ether was added to the residue to allow precipitation of crystals, and crystals were collected by filtration. A mixture of the obtained crystal, tetrahydrofuran (500 mL) and thionyl chloride (14.16 g) was heated under reflux for 2 hrs. The reaction mixture was concentrated and ethyl acetate was added to the residue. The ethyl acetate layer was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The obtained residue was subjected to silica gel column chromatography and eluted with ethyl acetate-hexane (1:6, v/v) to give ethyl 5-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)thiophene-2-carboxylate as colorless crystals (5.41 g, yield 24%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 101-102° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07368578B2 |
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| 출처 데이터셋 | uspto-grants-2008_05 |
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| ORD ID | ord-153c4d47d5ca4274ba664f148409f6ca |
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| 출처 메모 | uspto-grants-2008_05 |
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