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HRID 25015作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物PyridineHCID 1049—
反応物2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
反応物4-(2,6-Difluorobenzyloxy)benzylcarbonyl chlorideHCID 21964509—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 4-(4-(2,6-difluorobenzyloxy)phenyl)-3-oxobutyrateHCID 21964507—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858602B2
出典データセットuspto-grants-2005_02
ORD IDord-0e41a935a22a43f7b0ecc02577376e47
出典メモuspto-grants-2005_02