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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242290Generated: October 26, 2026

1,2-Dimethoxyethane → 5,5'-Bis[4-(octyloxy)phenyl]-2,2'-bithiophene

https://huagongshe.com/reaction/2242290

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant5,5'-Dibromo-2,2'-bithiopheneHCID 638908—
Reactant4-n-Octyloxyphenylboronic Acid (contains varying amounts of Anhydride)HCID 3977284—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
Product5,5'-Bis[4-(octyloxy)phenyl]-2,2'-bithiopheneHCID 59027319—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of 4-octyloxy-phenylboronic acid (Compound 7) (12.0 g, 0.048 mol), 5,5′-dibromo-2,2′-bithiophene (Compound 8) (7.23 g, 0.022 mol), bis(triphenylphosphine) palladium (II) dichloride (0.39 g, 0.56 mmol), and potassium phosphate (15.3 g, 0.072 mol), 160 mL ethylene glycol dimethylether and 50 mL water were added. After heating for 4 hours at 70° C., the reaction mixture was cooled on an ice bath. The solids were filtered and washed with a small amount of chloroform. The solids were suspended in 600 mL water, stirred for 30 minutes, and then filtered. This washing procedure was repeated with methanol. Following two crystallizations from trifluorotoluene using decolorizing charcoal, 5,5′-di(4-octyloxy-phenyl)-2,2′-bithiophene (Compound 4) was isolated as yellow/orange crystals (10.34 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671083B2
Source datasetuspto-grants-2010_03
ORD IDord-a505cfd53a394aa78ab6c2bc3d5c9449
Source noteuspto-grants-2010_03