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HRID 400644作成日:2026年10月26日

Allyl bromide → 2-Methyl-2-phenylpent-4-enenitrile

https://huagongshe.com/reaction/400644

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物2-PhenylpropionitrileHCID 15761—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
溶媒Dimethyl SulfoxideHCID 679—
溶媒TetrahydrofuranHCID 8028—
溶媒Ammonium ChlorideHCID 25517—
生成物2-Methyl-2-phenylpent-4-enenitrileHCID 1051137999.6%

反応手順

To a solution of 2-phenylpropionitrile (4.04 g, 30.79 mmol) in 40 mL of DMSO was added 34 mL (34 mmol) of a 1 M solution of sodium bis(trimethylsilyl)amide (NaHMDS) in THF over a 5 minute period. After 10 minutes, allyl bromide (6 mL, 69.33 mmol) was added dropwise (exothermic). The mixture was cooled with an ice-water bath. The mixture stirred for 20 minutes, becoming a solid mass. An additional 20 mL of DMSO was added. After 10 minutes, the mixture was diluted with 200 mL of ammonium chloride and extracted with three 100 mL portions of ethyl acetate. The combined organic layers were washed with six 75 mL portions of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 5.25 g (99.5% yield) of 2-methyl-2-phenylpent-4-enenitrile as yellow oil which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08741897B2
出典データセットuspto-grants-2014_06
ORD IDord-92b51de5a53942ec8f909e4ba5bb9eaf
出典メモuspto-grants-2014_06