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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049401Generated: October 31, 2026

Water → Ethyl 2-(3-(((2'-fluoro-5'-methoxy-2-neopentyl-[1,1'-biphenyl]-4-yl)oxy)methyl)phenoxy)acetate

https://huagongshe.com/reaction/1049401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2'-Fluoro-5'-methoxy-2-neopentyl-[1,1'-biphenyl]-4-olHCID 117759632—
ReactantEthyl 2-(3-(((methylsulfonyl)oxy)methyl)phenoxy)acetateHCID 117759824—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(3-(((2'-fluoro-5'-methoxy-2-neopentyl-[1,1'-biphenyl]-4-yl)oxy)methyl)phenoxy)acetateHCID 11775986465.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ethyl 2-(3-(((methylsulfonyl)oxy)methyl)phenoxy)acetate (94 mg) and 2′-fluoro-5′-methoxy-2-neopentyl-[1,1′-biphenyl]-4-ol (120 mg) in DMF (3.0 mL) was added potassium carbonate (67 mg), and the mixture was stirred at 80° C. for 3 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (102 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382188B2
Source datasetuspto-grants-2016_07
ORD IDord-4cf2dad564b8422e88e8297f0db8d3de
Source noteuspto-grants-2016_07