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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 5,5'-Dibromo-2,2'-bithiophene | HCID 638908 | — |
| Reactant | 4-n-Octyloxyphenylboronic Acid (contains varying amounts of Anhydride) | HCID 3977284 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,5'-Bis[4-(octyloxy)phenyl]-2,2'-bithiophene | HCID 59027319 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07671083B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-a505cfd53a394aa78ab6c2bc3d5c9449 |
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| Source note | uspto-grants-2010_03 |
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