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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026569Generated: October 31, 2026

Dimethylformamide → benzyl 2'-{[(2S)-3-{[tert-butyl(diphenyl)silyl]oxy}-2-methylpropyl]oxy}-3-fluorobiphenyl-4-carboxylate

https://huagongshe.com/reaction/1026569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
ReactantBenzyl 3-fluoro-2'-hydroxybiphenyl-4-carboxylateHCID 68005717—
Reactant((R)-3-bromo-2-methylpropoxy)-tert-butyldiphenylsilaneHCID 69007455—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Productbenzyl 2'-{[(2S)-3-{[tert-butyl(diphenyl)silyl]oxy}-2-methylpropyl]oxy}-3-fluorobiphenyl-4-carboxylateHCID 6800651376.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To an N,N-dimethylformamide solution (30 ml) of benzyl 3-fluoro-2′-hydroxybiphenyl-4-carboxylate (Example 1-3) (1.0 g) and {[(2R)-3-bromo-2-methylpropyl]oxy}(tert-butyl)diphenylsilane (1.5 g) was added at room temperature cesium carbonate (2.4 g), followed by stirring at 60° C. for 1 hour. Ethyl acetate and water were added to the reaction solution, and the solution was separated. The organic layer was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to afford benzyl 2′-{[(2S)-3-{[tert-butyl(diphenyl)silyl]oxy}-2-methylpropyl]oxy}-3-fluorobiphenyl-4-carboxylate (1.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729095B2
Source datasetuspto-grants-2014_05
ORD IDord-2cb2a03b3df64b99bead2feb82365b60
Source noteuspto-grants-2014_05