HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295477Generated: October 30, 2026
Dichlorodimethylsilane → Dimethyl(2-methyl-4-phenylindenyl)silyl chloride
https://huagongshe.com/reaction/1295477
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichlorodimethylsilane | HCID 6398 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-Methyl-4-phenylindene | HCID 11074559 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Dimethyl(2-methyl-4-phenylindenyl)silyl chloride | HCID 21943894 | 92.8% |
Reaction Steps
A 2.5 M solution of n-BuLi in hexane (4.85 mL, 12.12 mmol) was added at 0° C. to a solution of 2.50 g of 2-methyl-4-phenyl-indene (Boulder Scientific Company, Mw=206.29, 12.12 mmol, n-BuLi:2-Me-4-Ph-Ind=1:1) in 30 mL of ether. The resulting mixture was stirred for additional 2 h at room temperature with final formation of an orange solution. This solution was cooled again to 0° C. and added slowly of a solution of 1.58 mL of dichlorodimethylsilane (Aldrich, Mw=129.06, d=1.064, 13.03 mmol, Me2SiCl2:2-Me-4-Ph-Ind=1.08:1) in 20 mL of ether. The reaction mixture was then allowed to warm up to room temperature and stirred for 1 h. The final straw yellow suspension was concentrated under vacuum and the residue was extracted with 50 mL of toluene. The extract was dried under vacuum to give 3.36 g of a straw yellow solid, which was characterized by GC-MS analysis and 1H-NMR spectroscopy. Yield=92.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07241903B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-0ede1a6abc00468ba045eea616ac02ec |
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| Source note | uspto-grants-2007_07 |
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