HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399959Generated: October 26, 2026
Chlorotrimethylsilane → Tris(4-tert-butoxyphenyl)sulfonium chloride
https://huagongshe.com/reaction/399959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Chloro-4-tert-butoxybenzene | HCID 140458 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Bis(4-tert-butoxyphenyl) sulfoxide | HCID 15389810 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tris(4-tert-butoxyphenyl)sulfonium chloride | HCID 85759090 | 35% |
Reaction Steps
A solution of 17.8 g (0.052 mol) of bis(4-tertbutoxyphenyl) sulfoxide in 52 g of THF was cooled on an ice bath. To the solution, 5.3 g (0.052 mol) of triethylamine was added and 14.1 g (0.13 mol) of trimethylsilyl chloride was dropwised at 0° to 10° C. Stirring was continued at 0 to 10° C. for 30 minutes. To this solution, a Grignard reagent which was conventionally prepared from 24.0 g (0.13 mol) of 4-tert-butoxychlorobenzene, 3.2 g (0.13 mol) of magnesium, and 40 g of THF was dropwised at 0° to 10° C. Stirring was continued at 0° to 10° C. for 30 minutes. 300 g of 20% ammonium chloride aqueous solution was added to the reaction mixture. To the organic layer was added 500 g of chloroform. The organic layer was washed twice with 200 g of water and the solvent was evaporated and residue was purifie by column chromatography (silica gel, eluent: chloroform/methanol), isolating 9.3 g (yield 35%) of tris(4-tert-butoxyphenyl)sulfonium chloride with 99% purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05824824 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-e721bbc8b2e044319a53e787de2ae595 |
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| Source note | uspto-grants-1998_10 |
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