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HRID 852976作成日:2026年10月25日

Ammonium Chloride → 1-(Allyldimethylsilanyl)-4-trimethylsilanylethynyl benzene

https://huagongshe.com/reaction/852976

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物AllylchlorodimethylsilaneHCID 77646—
反応物(4-Bromophenylethynyl)trimethylsilaneHCID 4226980—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物1-(Allyldimethylsilanyl)-4-trimethylsilanylethynyl benzeneHCID 1218405293.3%

反応手順

6.4 mL (10 mmol) of a 1.6 M hexane solution of butyl lithium was added to 60 mL of THF solution containing 2.54 g (10 mmol) of (4-bromo-phenylethynyl)trimethyl silane under an argon atmosphere at a temperature of −78° C. and the resultant mixture was stirred for 30 minutes. Then, 1.5 mL (10 mmol) of allylchlorodimethyl silane was added to the mixture and stirred for 10 minutes, after which the temperature of the mixture was gradually returned to room temperature and additionally stirred for two hours. After an aqueous solution of ammonium chloride was added to the mixture, the resultant solution was subjected to extraction using ether. The organic layer thus created was then washed with saturated brine and dried using magnesium sulfate as a desiccating agent. After the desiccating agent was removed by filtration, the solvent was removed by a rotary evaporator to obtain a crude product, which was then purified by silica gel column chromatography (developing solvent: hexane) to obtain 2.54 g (9.33 mmol) of 1-(allyldimethylsilanyl)-4-trimethylsilanylethynyl benzene. The yield was 93%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07253243B2
出典データセットuspto-grants-2007_08
ORD IDord-e2bf638c0ba840c7b69d7cc6a8a7b726
出典メモuspto-grants-2007_08