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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485103Generated: October 31, 2026

Triethylsilane → HCID 178502736, compound

https://huagongshe.com/reaction/1485103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactantbismuth(III) bromideHCID 82232—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178502738HCID 178502738—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 178502736HCID 17850273662.3%

Reaction Steps

To a solution in acetonitrile (11 mL) of the compound (1.00 g) obtained in step (2) above, triethylsilane (579 mg) was added. Bismuth tribromide (104 mg) and 4-fluorobenzaldehyde (617 mg) were added under cooling with ice and the mixture was stirred at room temperature for two hours. To the reaction mixture, a saturated aqueous solution of sodium hydrogencarbonate and ethyl acetate were added and the insoluble matter was removed by filtration through Celite (registered trademark). The organic layer in the filtrate was separated and washed with saturated brine. The washed organic layer was dried over anhydrous magnesium sulfate and after removing the desiccant by filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=100:0-50:50) to give the titled compound as a colorless oil (0.61 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422240B2
Source datasetuspto-grants-2016_08
ORD IDord-54906bf9c1934e50b9a2d1814099c01c
Source noteuspto-grants-2016_08