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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216716Generated: October 31, 2026

Dichlorodimethylsilane → Dimethyl(2-methyl-4-phenylindenyl)silyl chloride

https://huagongshe.com/reaction/2216716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichlorodimethylsilaneHCID 6398—
ReactantHexaneHCID 8058—
Reactant2-Methyl-4-phenylindeneHCID 11074559—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductDimethyl(2-methyl-4-phenylindenyl)silyl chlorideHCID 2194389492.8%

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 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112638B2
Source datasetuspto-grants-2006_09
ORD IDord-b18473d95c754a5895d2f865aaea420d
Source noteuspto-grants-2006_09