HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403144Generated: October 29, 2026
Potassium Carbonate → (3-Bromophenyl)(3-(dibenzo[b,d]thiophen-4-yl)phenyl)diphenylsilane
https://huagongshe.com/reaction/403144
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bis(3-bromophenyl)diphenylsilane | HCID 297508 | — |
| Reactant | Dibenzothiophene-4-boronic acid | HCID 2734329 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (3-Bromophenyl)(3-(dibenzo[b,d]thiophen-4-yl)phenyl)diphenylsilane | HCID 86674047 | 62.4% |
Reaction Steps
A mixture solution of dibenzo[b,d]thiophen-4-boronic acid (1.84 g, 8.04 mmol), bis(3-bromophenyl)diphenylsilane (9.97 g, 20.17 mmol), Pd(PPh3)4 (0.19 g, 0.16 mmol) and potassium carbonate (6.69 g, 48.4 mmol,) in toluene (60 mL) and water (20 mL) was heated at 100° C. under nitrogen overnight. After cooling to room temperature, the reaction mixture was quenched with water, extracted with DCM, washed with brine and water, and dried over Na2SO4. Upon evaporation of the solvent, the residue was purified by column chromatography on silica gel with hexane:DCM (9.5:0.5 to 9:1, v/v) as eluent. The crude product was dissolved in DCM, precipitated with methanol, and filtered to yield (3-bromophenyl)(3-(dibenzo[b,d]thiophen-4-yl)phenyl)diphenylsilane (3.0 g, 62%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748012B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-1ca454cc9a5e4d299524ffad7e5ab365 |
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| Source note | uspto-grants-2014_06 |
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