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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253255생성일: 2026년 10월 25일

Potassium Cyanide → (2-(Methyloxy)-3-{[2-(methyloxy)ethyl]oxy}phenyl)acetonitrile

https://huagongshe.com/reaction/253255

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CyanideHCID 9032—
반응물1-(Chloromethyl)-2-(methyloxy)-3-{[2-(methyloxy)ethyl]oxy}benzeneHCID 66890780—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(2-(Methyloxy)-3-{[2-(methyloxy)ethyl]oxy}phenyl)acetonitrileHCID 6689025854.3%

반응 조건

온도60 °C

반응 단계

1-(Chloromethyl)-2-(methyloxy)-3-{[2-(methyloxy)ethyl]oxy}benzene (0.33 g, 1.4 mmol) was dissolved in N,N-dimethylformamide (2 mL) followed by the addition potassium cyanide (0.12 g, 1.6 mmol), and the resulting mixture was heated at 60° C. for 18 hours. After cooling to room temperature, it was diluted with ethyl acetate (50 mL), washed with water and brine (20 mL each), dried over sodium sulfate, filtered and concentrated to give an oily residue which was purified by flash chromatography (50% ethyl acetate/hexanes) to provide (2-(methyloxy)-3-{[2-(methyloxy)ethyl]oxy}phenyl)acetonitrile (0.17 g, 0.76 mmol, 54% yield). 1H NMR (400 MHz, CDCl3): 7.03-7.00 (d, d, 1H), 6.95-6.89 (m, 2H), 4.16-4.14 (m, 2H), 3.94 (s, 3H), 3.79-3.77 (m, 2H), 3.70 (s, 2H), 3.44 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872014B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-4619461f5b344fdbae0a49b6b7b4042f
출처 메모uspto-grants-2011_01