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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichlorodimethylsilane | HCID 6398 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | n-Methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indole | HCID 22722361 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178420856 | HCID 178420856 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Chlorodimethyl(n-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indol-6-yl)silane | HCID 22722352 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06730754B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-9d14bcbd2f9441b0b3c7912e56b43b56 |
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| Source note | uspto-grants-2004_05 |
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