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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090539Generated: October 25, 2026

N-Iodosuccinimide → (E)-(1-(4-methoxyphenyl)-2-(5-methyl-2-thienyl)ethenyl)-bis(2,4,6-trimethylphenyl)borane

https://huagongshe.com/reaction/2090539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantDimesitylboron fluorideHCID 3466040—
Reactant(Z)-(1-(4-methoxyphenyl)-2-(5-methyl-2-thienyl)-ethenyl)trimethylsilaneHCID 58159983—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Product(E)-(1-(4-methoxyphenyl)-2-(5-methyl-2-thienyl)ethenyl)-bis(2,4,6-trimethylphenyl)boraneHCID 66931403—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a nitrogen atmosphere, N-iodosuccinimide (1.1 g, 5.0 mmol) was added to an acetonitrile solution of (Z)-(1-(4-methoxyphenyl)-2-(5-methyl-2-thienyl)-ethenyl)trimethylsilane (0.3 g, 1.0 mmol) at 0° C. The mixture was stirred for 5 hours while maintaining at 0° C., and then applied to an alumina column for concentration. In a nitrogen atmosphere, the residue obtained was dissolved in diethyl ether, and n-butyl lithium (0.9 mL, 1.4 mmol) was added dropwise at −78° C. The mixture was stirred for 1 hour while maintaining at −78° C., and dimesityl boron fluoride (0.37 g, 1.56 mmol) was then added thereto. The mixture was stirred at room temperature for 12 hours, and water was then added thereto, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium chloride solution and then dried with magnesium sulfate, followed by filtration. The filtrate was concentrated, and the residue was purified by silica gel column chromatography (dichloromethane) and recrystallization (diethyl ether). Thus, (E)-(1-(4-methoxyphenyl)-2-(5-methyl-2-thienyl)ethenyl)-bis(2,4,6-trimethylphenyl)borane was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436173B2
Source datasetuspto-grants-2013_05
ORD IDord-61c5d3ba229b48c4935bfeb0015b8516
Source noteuspto-grants-2013_05