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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581734Generated: November 1, 2026

Dichlorodimethylsilane → Chlorodimethyl(n-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indol-6-yl)silane

https://huagongshe.com/reaction/1581734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichlorodimethylsilaneHCID 6398—
ReactantHexaneHCID 8058—
Reactantn-Methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indoleHCID 22722361—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178420856HCID 178420856—
SolventTetrahydrofuranHCID 8028—
ProductChlorodimethyl(n-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indol-6-yl)silaneHCID 22722352—

Reaction Conditions

Temperature-78 °C

Reaction Steps

3.4 mL of a 2.5 M solution of n-BuLi in hexane (8.50 mmol) were added dropwise to a solution of 2.22 g of N-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indole, obtained as reported above, (Mw=249.32, purity 85.8%, 7.64 mmol; indenoindole: n-BuLi=1:1.1) in 50 mL of THF, previously cooled to −78° C. At the end of the addition, the brown solution was allowed to warm up to room temperature and stirred for 5 hours. Then it was cooled again to −78° C. and added dropwise to a solution of dichlorodimethylsilane (Mw=129.06, d=1.064, 0.92 mL, 7.64 mmol; indenoindole: Me2SiCl2=1:1) in 20 mL of THF, previously cooled to −78° C. At the end of the addition, the dark brown solution was allowed to warm up to room temperature and stirred overnight. The solvents were evaporated under reduced pressure to give the desired product, containing few by-products, in the form of a brown sticky solid; this product was used in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730754B2
Source datasetuspto-grants-2004_05
ORD IDord-9d14bcbd2f9441b0b3c7912e56b43b56
Source noteuspto-grants-2004_05