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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 6-Methyl-4-phenyl-1,2,3,5-tetrahydro-s-indacene | HCID 53445346 | — |
| Reactant | Chloro-(2-i-propyl-4-phenyl-indenyl)-dimethylsilane | HCID 68744992 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | HCID 178418260 | HCID 178418260 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Dimethyl-(4-phenyl-6-methyl-1,2,3,5-tetrahydro-s-indacenyl)(2-i-propyl-4-phenyl-1-indenyl)-silane | HCID 68745586 | 104.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07452949B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-0655d291149141199cfe92ce5ecfcf50 |
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| Source note | uspto-grants-2008_11 |
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