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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1762318생성일: 2026년 10월 27일

2-Aminopropanol → ethyl 2-(3-acetyloxy-2,4,5-trifluorobenzoyl)-3-(1-hydroxypropan-2-ylamino)prop-2-enoate

https://huagongshe.com/reaction/1762318

반응식

참여 물질

역할이름HCID투입량
반응물2-AminopropanolHCID 5126—
반응물Acetic AnhydrideHCID 7918—
반응물Ethyl 3-acetoxy-2,4,5-trifluorobenzoylacetateHCID 13934696—
용매DichloromethaneHCID 6344—
생성물ethyl 2-(3-acetyloxy-2,4,5-trifluorobenzoyl)-3-(1-hydroxypropan-2-ylamino)prop-2-enoateHCID 178472010—

반응 단계

To 7.64 g (0.025 mole) of the ethyl 3-acetoxy-2,4,5-trifluorobenzoylacetate (VIII) thus obtained were added 20 ml of acetic anhydride and 6 ml of ortho-ethyl formate and the mixture was refluxed for 2 hours and then condensed under reduced pressure. The residue was dissolved in 50 ml of dichloromethane, added 1.91 g (0.026 mole) of DL-2-aminopropanol and allowed to stand over night. Dichloromethane was distilled under reduced pressure and the residue was applied to silica gel column chromatography (solvent: mixture of toluene:ethyl acetate=1:1) to give 4.37 g of the ethyl-2-(3-acetoxy-2,4,5-trifluorobenzoyl)-3-(2-hydroxy-1-methylethyl)aminoacrylate (X) as pale yellow oily product. ##STR10##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04831190
출처 데이터셋uspto-grants-1989_05
ORD IDord-5fc6f5b5d4d840d8820924c181fb5983
출처 메모uspto-grants-1989_05