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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25476생성일: 2026년 10월 24일

Acetic Acid → Methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetate

https://huagongshe.com/ko/reaction/25476

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2-ChlorobenzaldehydeHCID 6996—
반응물PiperidineHCID 8082—
반응물Methyl 4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)-3-oxobutanoateHCID 22568398—
용매IsopropanolHCID 3776—
생성물Methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetateHCID 69267975—

반응 조건

온도37.5 °C

반응 단계

85 g of methyl 4-(2-(phthalimido)ethoxy)acetoacetate was agitated with 31.7 ml of 2-chlorobenzaldehyde and 37 ml of 2-propanol at 20-25° C. The solution of 1.1 ml of piperidine in 14 ml of 2-propanol was added dropwise during 1.5 hour. The mixture was than agitated for 2 hours at the same temperature and for 2 hours at 35-40° C. The mixture was acidified with 1.5 ml of acetic acid, 140 ml of 2-propanol was added and the solution was cooled to 0-5° C. The isopropanolic layer was separated and the organic layer was again washed with 53 ml of 2-propanol. The organic layer, containing the desired product, was evaporated to dryness in order to remove the residual solvent.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858738B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-f4363df668ef423ea1801561f3f5fbda
출처 메모uspto-grants-2005_02