Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 977245생성일: 2026년 10월 26일
Hydrochloric Acid → 2-Hydroxy-4-[4-[3-(5-methyl-2-phenyl-4-oxazolyl) propionyl)phenyl]butyric acid
https://huagongshe.com/reaction/977245
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | 1,4-Dioxane | HCID 31275 | — |
| 반응물 | 2-Acetoxy-4-[4-[3-(5-methyl-2-phenyl-4-oxazolyl)propionyl]phenyl]butyronitrile | HCID 19965643 | — |
| 생성물 | 2-Hydroxy-4-[4-[3-(5-methyl-2-phenyl-4-oxazolyl) propionyl)phenyl]butyric acid | HCID 19965614 | — |
반응 단계
A mixture of 2-acetoxy-4-[4-[3-(5-methyl-2-phenyl-4-oxazolyl)propionyl]phenyl]butyronitrile (1.72 g), 6 N HCl (20 ml) and dioxane (10 ml) was heated under refluxing conditions for 3 hours. The reaction mixture was poured over water and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4) and then concentrated under reduced pressure to yield 2-hydroxy-4-[4-[3-(5-methyl-2-phenyl-4-oxazolyl) propionyl)phenyl]butyric acid as a solid substance. The solid was dissolved in ethanolic hydrogen chloride (10%, w/w, 20 ml), followed by stirring at 75°-80° C. for 2 hours. The reaction mixture was poured over water and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4) and then concentrated under reduced pressure; the residue was subjected to silica gel column chromatography. From the fraction eluted with ethyl acetate-hexane (1:1), 2-hydroxy-4-[4-[3-(5-methyl-2-phenyl4-oxazolyl)propionyl]phenyl]butyric acid ethyl ester (1.54 g, 88%) was obtained, which was then recrystallized from dichloromethane-isopropyl ether to yield colorless needles having a melting point of 87°-88° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05614544 |
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| 출처 데이터셋 | uspto-grants-1997_03 |
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| ORD ID | ord-2c967835b7504568a80ed74758c5e913 |
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| 출처 메모 | uspto-grants-1997_03 |
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