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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 882090생성일: 2026년 10월 26일

Acetoacetic Acid → Acetoacetic Acid

https://huagongshe.com/reaction/882090

반응식

참여 물질

역할이름HCID투입량
반응물Acetoacetic AcidHCID 96—
반응물PyridineHCID 1049—
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물Acetoacetic AcidHCID 96—
생성물5-Ethyl-2-pyridineethanolHCID 78894—

반응 단계

Bromination of olefin 2 with bromine in a neutral solvent e.g. dichloromethane, carbon tetrachloride, can give 5. Similarly, cyclic sulfate 10a may be prepared via oxidation of cyclic sulfite 10b, which in turn may be obtained form diol 11 by reacting with thionyl chloride, in the presence of bases e.g. pyridine, triethylamine. The formation of diol 11, can be achieved from diacetate 17, by treatment with base in water or methanol or ethanol. Alternatively, one can also prepare diol 11, from the diacetate 17 which in turn can be obtained from N-oxide of 5-ethyl-2-pyridyl-2-ethanol as shown in scheme I. In all the above transformations (Scheme 1) upon completion of the reaction, the desired compound is easily isolated from the reaction mixture in a most conventional manner eg. extracting in organic layer, washing with water, drying organic layer, concentrating and purifying/crystallizing the desired final product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08993773B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-fb9148b2af49417ba8cafbe434ed2e9f
출처 메모uspto-grants-2015_03