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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079211Generated: October 30, 2026

Hydrochloric Acid → (2-Allyl-4-bromo-6-methoxyphenoxy)triisopropylsilane

https://huagongshe.com/reaction/2079211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantImidazoleHCID 795—
ReactantTriisopropylsilyl chlorideHCID 139400—
Reactant2-Allyl-4-bromo-6-methoxyphenolHCID 57407756—
Reactant4-({[2-fluoro-3-(2-fluoroethoxy)-5-methoxyphenyl]-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl}amino)benzamidine acetateHCID 136366262—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(2-Allyl-4-bromo-6-methoxyphenoxy)triisopropylsilaneHCID 67097015—

Reaction Conditions

Temperature50 °C

Reaction Steps

After dissolving 3g of 2-allyl-4-bromo-6-methoxy-phenol [CAS No. 352019-92-2] in 10 ml of DMF, 1.3 g of imidazole and 2g of chlorotriisopropylsilane were added and the mixture was stirred at 50° C. for 4 hours. Next, 1N hydrochloric acid was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off, and the filtrate was concentrated under reduced pressure to give (2-allyl-4-bromo-6-methoxyphenoxy)triisopropylsilane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928228B2
Source datasetuspto-grants-2011_04
ORD IDord-9d13c5536e954ff49aeaec60ebbdfc94
Source noteuspto-grants-2011_04