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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212413Generated: October 29, 2026

Hydrochloric Acid → HCID 21964518, compound

https://huagongshe.com/reaction/2212413

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—
ProductHCID 21964518HCID 21964518—

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 numberUS07101910B2
Source datasetuspto-grants-2006_09
ORD IDord-6917f8a3d74344b9827b75ec1d8b75a2
Source noteuspto-grants-2006_09