HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379903Generated: October 25, 2026
Dichlorodiphenylsilane → Trimethylsiloxydiphenylchlorosilane
https://huagongshe.com/reaction/2379903
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichlorodiphenylsilane | HCID 6627 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylsilanol | HCID 66110 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Trimethylsiloxydiphenylchlorosilane | HCID 19417892 | 71.4% |
Reaction Steps
The following were ingredients were introduced into a stirrer-equipped four-neck flask: 164.8 g (651.2 mmol) diphenyldichlorosilane and 300 mL tetrahydrofuran. The resultant mixture was stirred at room temperature while a mixture of 60 g (542.7 mmol) of 81.4% pure trimethylsilanol and 65.9 g (651.2 mmol) of triethylamine was added dropwise. Stirring at room temperature was continued for an additional hour following completion of the addition, at which time the salt formed as a by-product of the reaction was removed by filtration. The filtrate was then distilled under reduced pressure to yield 118.7 g of a fraction boiling at 136.5° C.-142° C. under of 2 mm Hg, equivalent to a 71.4% yield of trimethylsiloxydiphenylchlorosilane. Analysis of this product by gas chromatography (GLC), nuclear magnetic resonance (NMR), and infrared spectrochemical analysis (IR) confirmed it to be trimethylsiloxydiphenylchlorosilane with the following structural formula. ##STR6##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05364896 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-d4d30c271a5a413ab29ed7fb832db57c |
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| Source note | uspto-grants-1994_11 |
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