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HRID 4451作成日:2026年10月24日

2-Methyl-1-butanol → (s)-4-(6-Methyloctyloxy)benzonitrile

https://huagongshe.com/ja/reaction/4451

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-1-butanolHCID 8723—
反応物Potassium CarbonateHCID 11430—
反応物4-CyanophenolHCID 13019—
反応物1-Bromo-6-methyloctaneHCID 13548105—
溶媒DimethylformamideHCID 6228—
生成物(s)-4-(6-Methyloctyloxy)benzonitrileHCID 54307675—

反応手順

Add 5.75 g of 4-cyanophenol 10 g of 1 brom-6-methyl octane synthesized of available active amyl alcohol, 6.67 g of anhydrous potassium carbonate, 30 ml of N,N-dimethyl formamide into 100 ml four-mouth flask under nitrogen atmosphere, allow to react for 8 hours at 110° C. After the reaction, filter the insoluble matter, then extract ether. The organic layer is then washed with 5% NaOH, water and saturated salt water, then dried and evaporated to remove the ether. Then when the obtained oily matter is refined, 11.4 g of optical (s)-4-(6-methyloctyloxy)benzonitrile is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04725688
出典データセットuspto-grants-1988_02
ORD IDord-097ce1f06049442d8b63f92135cc032e
出典メモuspto-grants-1988_02