HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → tert-Butyldimethylsilyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-tert-Butyl-1,1,3,3,3-pentamethyldisiloxane | HCID 590017 | — |
| Product | Chlorotrimethylsilane | HCID 6397 | 79% |
| Product | tert-Butyldimethylsilyl chloride | HCID 28928 | 83.2% |
Reaction Steps
The reaction system was stirred at room temperature while dropwise adding thionyl chloride through the dropping funnel. In this manner, pentamethyl-t-butyl-disiloxane was reacted with thionyl chloride while dropwise adding the latter and supplying hydrogen chloride gas to the reaction solution. After stirring the reaction solution over 4 hours, it was distilled at 125° C. to give 31.3 g (yield 83.2%) of t-butyldimethylchlorosilane and 21.4 g (yield 79.0%) of trimethylchlorosilane. There was not observed the formation of any viscous oily substance, the distillation temperature during the purification could substantially be decreased and the post-treatment of the reaction vessel was very easy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05258537 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-4b27e93ff6fa47f3bf30ac2d431ceea1 |
| Source note | uspto-grants-1993_11 |