HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848829Generated: October 27, 2026
Cyclohexene → Cyclohexylphenethyldichlorosilane
https://huagongshe.com/reaction/848829
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | Monophenethyldichlorosilane | HCID 123907249 | — |
| Catalyst | Chloroplatinic acid | HCID 61859 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Cyclohexylphenethyldichlorosilane | HCID 54253331 | 60.7% |
Reaction Steps
Then into a 100 ml pressure-proof stainless steel reactor; 6.21 g (30.3 millimol) of the above-mentioned phenethyldichlorosilane, 4.47 g (54.4 millimol) of cylcohexene and 0.1 ml of a chloroplatinic acid solution in isopropanol (0.03 mol % relative to phenethyldichlorosilane) were charged and sealed. Reaction was carried out in an oil bath at 100° C. with stirring for 17.5 hours. After completion of reaction, the reacted solution was subjected to vacuum distillation to obtain 5.30 g (18.4 millimol) of cyclohexylphenethyldichlorosilane. This cyclohexylphenethyldichlorosilane had a boiling point of 112.8°~115.4° C./2.0 mmHg. The infrared spectrum of this compound is shown in FIG. 4. There is no characteristic absorption of Si-H at 2100 cm-1. The NMR spectrum is shown in FIG. 9. There are signals of δ value at 1.0~2.0 ppm (Si--CH2 and C--CH2 --); 2.4~3.0 ppm (--CH2 --C6H5) and 7.15 ppm (--C6H 5). The integral ratio thereof was 14:2:5. In the mass spectrum analysis, parent ion was M+ 286.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04297499 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-a1f0695eff4a42e5bad5663368b19f22 |
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| Source note | uspto-grants-1981_10 |
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