HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716445Generated: October 30, 2026
Water → (6-tert-Butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)-(6-tert-butyl-2-methyl-4-phenyl-1H-inden-1-yl)dimethylsilane
https://huagongshe.com/reaction/716445
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | (6-tert-Butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)(chloro)dimethylsilane | HCID 71231037 | — |
| Reactant | 5-tert-butyl-2-methyl-7-phenyl-1H-indene | HCID 86727905 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | HCID 178418546 | HCID 178418546 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (6-tert-Butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)-(6-tert-butyl-2-methyl-4-phenyl-1H-inden-1-yl)dimethylsilane | HCID 71231013 | 72.4% |
Reaction Steps
To a solution of 14.5 g (55.4 mmol) of 5-tert-butyl-2-methyl-7-phenyl-1H-indene in 400 ml of ether cooled to −78° C., 22.2 ml (55.5 mmol) of 2.5 M nBuLi in hexanes was added. This mixture was stirred overnight at room temperature, then cooled to −78° C., and 200 mg (2.23 mmol) of CuCN was added. The resulting mixture was stirred for 30 min at −20° C., then cooled to −78° C., and a solution of 21.2 g (55.4 mmol) of (6-tert-butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)(chloro)dimethylsilane in 200 ml of ether was added. This mixture was stirred overnight at room temperature, then 1 ml of water was added. The obtained mixture was passed through a short layer of silica gel 60 (40-63 um), the elute was evaporated to dryness. The product was isolated by flash-chromatography on silica gel 60 (40-63 um; eluent: hexanes-dichloromethane=10:1, vol., then 3:1, vol.). This procedure gave 24.5 g (72%) of yellowish glassy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187583B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-60e8b199e9fb4a70a743494eda8effb2 |
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| Source note | uspto-grants-2015_11 |
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