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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263450Generated: October 26, 2026

Hexane → (2-Methoxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane

https://huagongshe.com/reaction/2263450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDiethyldichlorosilaneHCID 15589—
Reactant1-Bromo-3-tert-butyl-2-methoxy-5-methylbenzeneHCID 617870—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product(2-Methoxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilaneHCID 11032947—

Reaction Steps

Under nitrogen atmosphere, 2-methoxy-1-bromo-3-tert-butyl-5-methylbenzene (20.00 g, 77.77 mmol) was dissolved in 200 mL of diethyl ether. A 1.57 M hexane solution of n-butyllithium (59.44 mL, 93.32 mmol) was dropwise added at −50° C. or lower, and a temperature was raised to room temperature, followed by stirring for 1 hour. All the amount of diethyldichlorosilane (24.44 g, 155.54 mmol) was added to the mixture at once at −50° C. or lower, and a temperature was gradually raised to room temperature. After being refluxed for 1 hour, the solution was concentrated under reduced pressure. Hexane was added, the insolubles were filtered off with a Celite filter, and the filtrate was concentrated under reduced pressure. Concentration was further continued at 70° C. under reduced pressure for 3 hours to obtain (2-methoxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane. Resultant (2-methoxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane was used in a subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851569B2
Source datasetuspto-grants-2010_12
ORD IDord-46884fa744ed402e90d94afd22542e10
Source noteuspto-grants-2010_12