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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25015생성일: 2026년 10월 24일

Hydrochloric Acid → Ethyl 4-(4-(2,6-difluorobenzyloxy)phenyl)-3-oxobutyrate

https://huagongshe.com/ko/reaction/25015

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PyridineHCID 1049—
반응물2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
반응물4-(2,6-Difluorobenzyloxy)benzylcarbonyl chlorideHCID 21964509—
용매DichloromethaneHCID 6344—
생성물Ethyl 4-(4-(2,6-difluorobenzyloxy)phenyl)-3-oxobutyrateHCID 21964507—

반응 조건

온도0 °C

반응 단계

To a solution of Meldrum's acid (0.846 g, 5.8 mmol) in dichloromethane (5 ml) was added pyridine (2 ml) over a period of 10 minutes at 0° C. To this solution was added 4-(2,6-Difluorobenzyloxy)benzylcarbonyl chloride (Step D, 1.71 g, 5.7 mmol) in dichloromethane (5 ml), which resulted in an orange solution. The dark orange solution was stirred for 1 hour at 0° C., allowed to warm to room temperature and stirred for an additional hour. The reaction mixture was diluted with dichloromethane and poured onto 2M HCl and ice. The phases were separated and the aqueous phase was extracted twice with dichloromethane. The combined organic layers were washed twice with 2M HCl and brine, dried over Na2SO4, filtered and concentrated to a solid. The solid was suspended in abs EtOH (15 ml) and refluxed for 2.5 hours. The solvent was removed in vacuo to give a dark oil. The residue was purified by flash chromatography on silica gel column (hex:ethyl acetate, 2:1) to provide the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858602B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-0e41a935a22a43f7b0ecc02577376e47
출처 메모uspto-grants-2005_02