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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251546Generated: October 27, 2026

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

https://huagongshe.com/reaction/251546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
Reactant4-(2,6-Difluorobenzyloxy)benzylcarbonyl chlorideHCID 21964509—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-(4-(2,6-difluorobenzyloxy)phenyl)-3-oxobutyrateHCID 21964507—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863475B2
Source datasetuspto-grants-2011_01
ORD IDord-950b0aff5d8740f8a800bcb6da32e3b3
Source noteuspto-grants-2011_01