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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881752Generated: October 31, 2026

Cesium fluoride → HCID 86700856, compound

https://huagongshe.com/reaction/881752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
ReactantHCID 86700855HCID 86700855—
ReactantHCID 86700857HCID 86700857—
CatalystBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86700856HCID 8670085658%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of [1-(4-chloro-phenyl)-2-oxa-bicyclo[2.2.2]oct-4-yl]-acetic acid methyl ester (0.29 g, 0.984 mmol) and (5-tert-butyl-[1,3,4]oxadiazol-2-yl)-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amine (0.338 g, 0.984 mmol) in dioxane (8 ml) and water (0.8 ml), was added caesium fluoride (0.448 g, 2.95 mmol) and Pd(amphos)Cl2 (0.070 g, 0.098 mmol). The mixture was flushed with nitrogen for three times and heated at 90° C. for 16 hours. The reaction mixture was filtered, and the solid was washed with water (10 ml) and ethyl acetate (3 ml) to afford crude {1-[4′-(5-tert-butyl-[1,3,4]oxadiazol-2-ylamino)-biphenyl-4-yl]-2-oxa-bicyclo[2.2.2]oct-4-yl}-acetic acid methyl ester (0.27 g, 58%) as white solid. [MS+1] 476.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993619B2
Source datasetuspto-grants-2015_03
ORD IDord-e6b946e0cf4145bd96bd7488cbf3ba77
Source noteuspto-grants-2015_03