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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53171Generated: October 29, 2026

Chlorotrimethylsilane → HCID 15379438, compound

https://huagongshe.com/reaction/53171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantBenzyl BromideHCID 7498—
Reactant1,2-DibromoethaneHCID 7839—
Reactant6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-oneHCID 15926016—
CatalystZincHCID 23994—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15379438HCID 15379438—

Reaction Conditions

Temperature60 °C

Reaction Steps

Zinc (227 mg, 3.48 mmol) is suspended in tetrahydrofuran (10 ml) and 1,2-dibromoethane (0.22 ml, 0.2 mmol) is added. The mixture is heated at 60° C. for 3 minutes, the solution is allowed to cool until the temperature is 35° C., and trimethylsilyl chloride (0.06 ml, 0.5 mmol) is slowly added. Stirring is maintained for 30 minutes and then benzyl bromide (0.11 ml, 0.9 mmol) is added. Wait a further 30 minutes before introducing 6-bromo-3-methyloxazolo[4,5-b]pyridin-2(3H)-one (200 mg, 0.87 mmol) and tetrakis(triphenylphosphine)palladium (4 mg). Heat at 50° C. for 20 minutes. After the solution has been cooled, the zinc is removed by filtration, the flitrate is taken up in water, and then a 10% aqueous hydrochloric acid solution is added until the aqueous phase becomes clear. Extraction is carried out with dichloromethane. The organic phase is dried over magnesium sulfate and filtered, and then the solvent is evaporated off under reduced pressure. The title product is purified by chromatography on silica gel (eluant: dichloromethane). The yield obtained is 91%. ##STR51##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618819
Source datasetuspto-grants-1997_04
ORD IDord-b4a73ef744a14bab9fa46296894a21b5
Source noteuspto-grants-1997_04