Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | 1,1'-Sulfinylbis(4-chlorobenzene) | HCID 18329 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11983794 | HCID 11983794 | — |
Reaction Steps
Under a nitrogen atmosphere, 16.3 g (0.06 mol) of di(4-chlorophenyl)sulfoxide was dissolved in 250 ml dichloremethane. Into the resulting solution kept at 0 to 5° C., 10.8 g (0.10 mol) of trimethylchlorosilane was added dropwise; the mixture was stirred at 0° C. for 30 min. Thereafter, 200 g of a tetrahydrofuran (THF) solution of the Grignard reagent prepared by the usual process with 4-bromochlorobenzene (0.18 mol) was added dropwise over the period of 30 min into the reaction vessel cooled with 0 to 10° C. ice water. After agitated for one hr at 0° C., followed by another hr agitation at room temperature, the reaction solution was slowly poured into an aqueous solution containing 250 ml of an aqueous 12% hydrogen bromide solution and ice, then extracted with 250 ml dichloromethane. The extract was dried with sodium sulfate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110337B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-ce97125950ee49cb92d2c881177bc3e6 |
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| Source note | uspto-grants-2012_02 |
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