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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550235Generated: October 26, 2026

Triethylsilane → 2-(4-Bromonaphthalen-2-ylmethyl)-5-fluorobenzo[b]thiophene

https://huagongshe.com/reaction/550235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantSodium BicarbonateHCID 516892—
Reactant(4-Bromo-naphthalen-2-yl)-(5-fluorobenzo[b]-thiophen-2-yl)methanolHCID 67156712—
SolventDichloromethaneHCID 6344—
Product2-(4-Bromonaphthalen-2-ylmethyl)-5-fluorobenzo[b]thiopheneHCID 67156577215.5%

Reaction Steps

In a nitrogen stream, triethylsilane (0.18 ml, 2.11 mmol) and a boron trifluoride-diethyl ether complex (0.25 ml, 1.94 mmol) were added to a solution of (4-bromo-naphthalen-2-yl)-(5-fluorobenzo[b]-thiophen-2-yl)methanol (260 mg, 0.65 mmol) in methylene chloride (10 ml) at 0° C. and the mixture was stirred a room temperature for two hours. A saturated sodium hydrogen carbonate aqueous solution was added and the mixture was extracted with methylene chloride. The organic layer was washed with a saturated sodium chloride aqueous solution and dried (anhydrous magnesium sulfate), and then the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:100)] to obtain the title compound (520 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943748B2
Source datasetuspto-grants-2011_05
ORD IDord-6e649d73c71c447597e84b19ea0769e8
Source noteuspto-grants-2011_05