Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Dichlorodimethylsilane | HCID 6398 | — |
| Reactant | 7-Phenyl-1H-indene | HCID 12942386 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21188885 | HCID 21188885 | 62% |
Reaction Steps
18.7 cm3 (50 mmol) of a 20% strength solution of butyllithium in toluene were added at room temperature to a solution of 10 g (50 mmol) of 10 in 100 cm3 of H2)- and O2-free toluene and 5 ml of H2O- and O2-free THF, and the mixture was heated at 80° C. for 2 hours. The yellow suspension was subsequently cooled to 0° C. and 3.2 g (25 mmol) of dimethyldichlorosilane were added. The reaction mixture was heated at 80° C. for a further 1 hour and subsequently washed with 50 cm3 of H2O. The solvent was removed in vacuo, and the residue was recrystallized from heptane at −20° C. giving 6.7 g (62%) of 11 as colorless crystals (m.p. 109-110° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06242544B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-4f491f5f85ca49d9a63aaa0632259ef7 |
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| Source note | uspto-grants-2001_06 |
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