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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(6-tert-Butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)(chloro)dimethylsilaneHCID 71231037—
Reactant5-tert-butyl-2-methyl-7-phenyl-1H-indeneHCID 86727905—
ReactantButyllithiumHCID 178418339—
CatalystHCID 178418546HCID 178418546—
SolventDiethyl EtherHCID 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)dimethylsilaneHCID 7123101372.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187583B2
Source datasetuspto-grants-2015_11
ORD IDord-60e8b199e9fb4a70a743494eda8effb2
Source noteuspto-grants-2015_11