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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271796Generated: October 26, 2026

Ammonium Chloride → Dimethyl-(4-phenyl-6-methyl-1,2,3,5-tetrahydro-s-indacenyl)(2-i-propyl-4-phenyl-1-indenyl)-silane

https://huagongshe.com/reaction/271796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant6-Methyl-4-phenyl-1,2,3,5-tetrahydro-s-indaceneHCID 53445346—
ReactantChloro-(2-i-propyl-4-phenyl-indenyl)-dimethylsilaneHCID 68744992—
ReactantButyllithiumHCID 178418339—
CatalystHCID 178418260HCID 178418260—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductDimethyl-(4-phenyl-6-methyl-1,2,3,5-tetrahydro-s-indacenyl)(2-i-propyl-4-phenyl-1-indenyl)-silaneHCID 68745586104.3%

Reaction Steps

To 12.3 g (50 mmol) of 4-phenyl-6-methyl-1,2,3,5-tetrahydro-s-indacene (2b) and 150 mg (1.5 mmol) of copper cyanide (I) in 450 ml of diethylether was added dropwise at −70° C. 23 ml (57 mmol) of 2.5 M of n-butyllithium in n-hexane. The solution was slowly warmed to room temperature and stirred for 3 hrs at room temperature. Then to the solution was added at −70° C. 16.4 g (50 mmol) of chloro-(2-i-propyl-4-phenyl-indenyl)-dimethylsilane and the solution was warmed to room temperature and stirred for 5 hrs. The resulting back slurry solution was poured into an aqueous ammonium chloride solution and the organic layer was washed with brine, dried over sodium sulfate and the solvents were evaporated to give 28 g of crude product. This was purified by column chromatography (800 g of silica gel, 101 Heptane:CH2Cl2=5:1). Yield: 9.5 g (35%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452949B2
Source datasetuspto-grants-2008_11
ORD IDord-0655d291149141199cfe92ce5ecfcf50
Source noteuspto-grants-2008_11