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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400238Generated: November 2, 2026

Ethanol → HCID 59861212, compound

https://huagongshe.com/reaction/2400238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1,4-DibromonaphthaleneHCID 66521—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59861212HCID 59861212—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 114.38 g (400 mmol) of 1,4-dibromonaphthalene and 1 l of THF (absolute) is cooled to −78° C. under protective gas, 160 ml (400 mmol) of n-butyllithium (2.5M in n-hexane) are subsequently slowly added at this temperature, and the mixture is stirred at −78° C. for a further 30 h. A mixture of 52.3 ml (400 mmol) of chlorotrimethylsilane in 200 ml of THF (absolute) is added to the solution obtained in this way, and the mixture is slowly warmed to room temperature. After addition of 150 ml of EtOH and subsequently 300 ml of water, the organic phase is separated off, dried over magnesium sulfate and evaporated. The oil obtained in this way is distilled at 115-135° C. and 1.7 mbar, giving 80 g (286 mmol) (corresponding to 88% of theory) of the product having a purity of greater than 99.0% according to HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08795847B2
Source datasetuspto-grants-2014_08
ORD IDord-a5ff2a8054dc49f794f3cf9ceb627d96
Source noteuspto-grants-2014_08