Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Aminopropanol → ethyl 2-(3-acetyloxy-2,4,5-trifluorobenzoyl)-3-(1-hydroxypropan-2-ylamino)prop-2-enoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Aminopropanol | HCID 5126 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Ethyl 3-acetoxy-2,4,5-trifluorobenzoylacetate | HCID 13934696 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | ethyl 2-(3-acetyloxy-2,4,5-trifluorobenzoyl)-3-(1-hydroxypropan-2-ylamino)prop-2-enoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04831190 |
| 출처 데이터셋 | uspto-grants-1989_05 |
| ORD ID | ord-5fc6f5b5d4d840d8820924c181fb5983 |
| 출처 메모 | uspto-grants-1989_05 |