Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Bromo-4-iodobenzene | HCID 11522 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13033313 | HCID 13033313 | 81% |
Reaction Steps
At first, a mixture of 4-iodo-bromobenzene (2.60 g, 9.19 mmol), t-butylammoniumiodido (3.39 g, 9.18 mmol) and [Rh(cod)(CH3CN)2] (105 mg, 0.277 mmol) was added with dimethylformamide (DMF: 26 mL) and triethylamine (2.56 mL, 18.4 mmol). Then, triethoxysilane (1.87 mL, 10.1 mmol) was added dropwise thereto at 0° C. The resultant mixture was stirred under a nitrogen atmosphere at 80° C. for one hour to obtain a reaction mixture. Subsequently, a solvent in the reaction mixture was distilled with a vacuum pump. Under a nitrogen atmosphere, the residue was extracted with ether, filtered with celite, and concentrated to obtain a crude product. Thereafter, the crude product thus obtained was purified by Kugel distillation, and thereby 4-bromo-triethoxysilylbenzene was obtained (2.38 g, 81% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608673B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-27c1b379d735480aa22a61d061c7fa07 |
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| Source note | uspto-grants-2009_10 |
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