HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256748Generated: October 31, 2026
Hydrochloric Acid → tert-Butyldimethylsilyl chloride
https://huagongshe.com/reaction/256748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-tert-Butyl-1,1,3,3,3-pentamethyldisiloxane | HCID 590017 | — |
| Product | Chlorotrimethylsilane | HCID 6397 | 80.2% |
| Product | tert-Butyldimethylsilyl chloride | HCID 28928 | 86.4% |
Reaction Steps
To a 1.0 l volume reaction vessel equipped with a stirring machine, a reflux condenser, a dropping funnel and an inlet pipe for hydrogen chloride gas, there were added 204 g (1.0 mole) of pentamethyl-t-butyl-disiloxane and 9.25 g (0.050 mole) of tributylamine and 143 g (1.2 mole) of thionyl chloride was introduced into the dropping funnel. Pentamethyl-t-butyl-disiloxane was reacted with thionyl chloride at room temperature by dropwise adding thionyl chloride through the dropping funnel while supplying hydrogen chloride gas to the reaction solution. After stirring over 4 hours, the reaction solution was distilled at 125° C. to give 130 g (yield 86.4%) of t-butyldimethylchlorosilane and 87.0 g (yield 80.2%) 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 |
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| Patent number | US05258537 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-e8c96d9645f8440d8c33aa9bb5accac5 |
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| Source note | uspto-grants-1993_11 |
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