HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425306Generated: October 28, 2026
Dichlorodimethylsilane → HCID 59735669, compound
https://huagongshe.com/reaction/2425306
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichlorodimethylsilane | HCID 6398 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | 2,4,6-trimethyl-1H-indene | HCID 10920786 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59735669 | HCID 59735669 | 97.5% |
Reaction Steps
A 2.5 M n-BuLi solution in hexane (37.2 mL, 0.093 mol) was added dropwise at 0° C. under nitrogen to a solution of 14.00 g of 2,4,6-trimethylindene (0.088 mol) in 100 mL of Et2O in a 500 mL 3-necked round flask. During the addition a white suspension was formed. The mixture was then allowed to warm up to r.t. and stirred for 30 min, with final formation of a white suspension. Then a solution of Me2SiCl2 (11.28 mL, 0.093 mol.) in 30 mL of THF was cooled to 0° C. and slowly added to the lithium salt suspension, also cooled to 0° C. The reaction mixture was allowed to warm up to r.t. and stirred for 2 h with final formation of a light yellow suspension. Then the solvents were removed in vacuo and the residue was extracted with 150 mL of toluene to remove LiCl. The light yellow filtrate was brought to dryness in vacuo to give 21.53 g of a yellow oil: its 1H-NMR analysis showed the presence of the target product together with traces of starting 2,4,6-trimethyl-indene (yield 97.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964679B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-429a9a155dee452f8e22dc21ea4777e8 |
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| Source note | uspto-grants-2011_06 |
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