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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28265생성일: 2026년 10월 23일

Phenethyl bromide → alpha-Phenethyl-2,4-dichlorobenzyl cyanide

https://huagongshe.com/ko/reaction/28265

반응식

참여 물질

역할이름HCID투입량
반응물Phenethyl bromideHCID 7666—
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물2,4-DichlorophenylacetonitrileHCID 80566—
용매WaterHCID 962—
생성물alpha-Phenethyl-2,4-dichlorobenzyl cyanideHCID 12391165—

반응 조건

온도30 °C

반응 단계

Sodium hydride (0.13 mole as a 50% dispersion in mineral oil) is washed with 100 ml. of dry n-hexane to remove the mineral oil, then blanketed with dry nitrogen and suspended in 250 ml. of freshly distilled tetrahydrofuran. To this sodium hydride suspension is added dropwise at room temperature a solution of 2,4-dichlorobenzyl cyanide (25 g., 0.13 mole) dissolved in 100 ml. of tetrahydrofuran. When the addition is completed, the temperature is maintained at 30° C. for an additional 0.5 hours. A solution of phenethylbromide (26 g., 0.14 mole) is then added dropwise and the resultant reaction mixture is stirred at 40° C. overnight under nitrogen. The reaction mixture is poured into 1 liter of water and extracted with (3×200 ml.) of ether. The combined ether extracts are washed with water, dilute hydrochloric acid, saturated sodium bicarbonate solution, saturated sodium chloride solution and dried over magnesium sulfate. The solvent is evaporated and the crude product distilled (144°-56°/0.03 mm) to give 26.6 g. (70.5%) of product, which is identified by nmr.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04225723
출처 데이터셋uspto-grants-1980_09
ORD IDord-c3178ad2e2c04db1a384f9147e3a6c47
출처 메모uspto-grants-1980_09