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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256748Generated: October 31, 2026

Hydrochloric Acid → tert-Butyldimethylsilyl chloride

https://huagongshe.com/reaction/256748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTributylamineHCID 7622—
ReactantThionyl ChlorideHCID 24386—
Reactant1-tert-Butyl-1,1,3,3,3-pentamethyldisiloxaneHCID 590017—
ProductChlorotrimethylsilaneHCID 639780.2%
Producttert-Butyldimethylsilyl chlorideHCID 2892886.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258537
Source datasetuspto-grants-1993_11
ORD IDord-e8c96d9645f8440d8c33aa9bb5accac5
Source noteuspto-grants-1993_11