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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550241Generated: October 30, 2026

Methanol → 2-(4-Bromo-1-methoxynaphthalen-2-yl-methyl)benzo[b]thiophene

https://huagongshe.com/reaction/550241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantTriethylsilaneHCID 12052—
ReactantBenzo[b]thiophen-2-yl-(4-bromo-1-methoxynaphthalen-2-yl)methanolHCID 67156311—
SolventDichloromethaneHCID 6344—
Product2-(4-Bromo-1-methoxynaphthalen-2-yl-methyl)benzo[b]thiopheneHCID 6660819380%

Reaction Steps

In a nitrogen stream, triethylsilane (2.48 ml, 15.5 mmol) and a boron trifluoride-diethyl ether complex (1.08 ml, 8.54 mmol) were added dropwise to a solution of benzo[b]thiophen-2-yl-(4-bromo-1-methoxynaphthalen-2-yl)methanol (3.1 g, 7.76 mmol) in methylene chloride (60 ml) at 0° C. and the reaction mixture was stirred at room temperature for two hours, and then a 50% methanol aqueous solution (1 ml) was added and furthermore water (30 ml) was added thereto. The resulting mixture was extracted with methylene chloride, and 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 (1:50)] to obtain the title compound (2.38 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943748B2
Source datasetuspto-grants-2011_05
ORD IDord-eb65cff3a7e047a2abf5ebc044186c82
Source noteuspto-grants-2011_05