HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52749Generated: October 29, 2026
Chlorotrimethylsilane → HCID 131719955, compound
https://huagongshe.com/reaction/52749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Hydroxybenzocyclobutene | HCID 21425209 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 131719955 | HCID 131719955 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616765 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-ca63de2d7e9a419c8f139687c0eb9182 |
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| Source note | uspto-grants-1997_04 |
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