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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52749Generated: October 29, 2026

Chlorotrimethylsilane → HCID 131719955, compound

https://huagongshe.com/reaction/52749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant4-HydroxybenzocyclobuteneHCID 21425209—
SolventBenzeneHCID 241—
ProductHCID 131719955HCID 13171995576%

Reaction Conditions

Temperature5 °C

Reaction Steps

A larger batch of 4-trimethylsiloxybenzocyclobutene was synthesized from 6.56 gms of 4-hydroxybenzocyclobutene and 5.54 gms of triethylamine, taken up in 15 ml anhydrous benzene followed by the addition of a nearly three molar excess of chlorotrimethylsilane (20 ml in 15 ml dry benzene) to the reaction mixture maintained at 5° C. An instant white precipitation of triethylamine hydrochloride was observed. The solution was allowed to warm up on its own to 15° C. in about 5 hours and the reaction mixture was kept stirred overnight, It was warmed to 40° C. and maintained for about three hours. The reaction mixture was cooled and the isolation of the product was done exactly as described before. The weight of the light yellow oil (crude) was 7.93 g, 76% yield. Total amount of the colorless oil obtained from vacuum distillation was 7.07 grams. Anal. Calc.: C, 68.69%; H, 8.38%. Found: C, 69.15%; H, 8.44%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616765
Source datasetuspto-grants-1997_04
ORD IDord-ca63de2d7e9a419c8f139687c0eb9182
Source noteuspto-grants-1997_04