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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400644생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/400644

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물2-PhenylpropionitrileHCID 15761—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
용매Dimethyl SulfoxideHCID 679—
용매TetrahydrofuranHCID 8028—
용매Ammonium ChlorideHCID 25517—
생성물2-Methyl-2-phenylpent-4-enenitrileHCID 1051137999.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741897B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-92b51de5a53942ec8f909e4ba5bb9eaf
출처 메모uspto-grants-2014_06