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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486377Generated: October 26, 2026

Potassium Carbonate → 2,2'-(5-(8-(4-(9H-carbazol-9-yl)phenyl)dibenzo[b,d]furan-2-yl)-1,3-phenylene)bis(benzo[d]oxazole)

https://huagongshe.com/reaction/1486377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant3,5-Bis(benzo[d]oxazol-2-yl)phenylboronic Acid Pinacol EsterHCID 86711728—
Reactant9-(4-(8-bromodibenzo[b,d]furan-2-yl)phenyl)-9H-carbazoleHCID 117607253—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Product2,2'-(5-(8-(4-(9H-carbazol-9-yl)phenyl)dibenzo[b,d]furan-2-yl)-1,3-phenylene)bis(benzo[d]oxazole)HCID 117607260—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of Compound 13 (1.00 g, 2.28 mmol), 2,2′-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-phenylene)bis(benzo[d]oxazole) (1.159 g, 2.37 mmol), tetrakis(triphenylphosphine) palladium(0) (0.13 g, 0.11 mmol), potassium carbonate (0.95 g, 6.85 mmol), 1,4-dioxane (20.00 mL), and water (4.00 mL) was degassed with bubbling argon for 20 minutes at 45° C. The reaction was then heated to 100° C. and stirred overnight (16.5 hours), maintaining an argon atmosphere. The precipitated product was filtered, dried, and performed boiling ethyl acetate, chloroform, and methanol washes. The solid product was collected to yield Host-7 (0.75 g, 45%). Confirmed by LCMS (APCI): calculated for C50H29N3O3 (M+H): 720. Found: 720.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09425408B2
Source datasetuspto-grants-2016_08
ORD IDord-d5b0144f6583400795a271f0094c36c1
Source noteuspto-grants-2016_08