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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 986915생성일: 2026년 10월 23일

Chloroacetonitrile → 2-(4-Fluorophenoxy)acetonitrile

https://huagongshe.com/ko/reaction/986915

반응식

참여 물질

역할이름HCID투입량
반응물ChloroacetonitrileHCID 7856—
반응물4-FluorophenolHCID 9732—
반응물Potassium CarbonateHCID 11430—
생성물2-(4-Fluorophenoxy)acetonitrileHCID 278305884%

반응 단계

A mixture of 4-fluorophenol (22.4 g, 200 mmol), chloroacetonitrile (17.1 g, 220 mmol) and excess powdered potassium carbonate was refluxed for 7 h then the mixture was concentrated under reduced pressure. The residue was mixed with H2O and was extracted with Et2O. The combined organic layers were dried, filtered and concentrated under reduced pressure. The residue was Kugelrohr distilled to provide 2-(4-Fluorophenoxy)acetonitrile (25 g, 84%). The 2-(4-Fluorophenoxy)acetonitrile (25 g, 185 mmol) was reduced with alane [generated from lithium aluminum hydride (19.6 g, 516 mmol) and sulfuric acid (25.3 g, 258 mmol) according to the procedure in Example 1]. The crude product was purified by Kugelrohr distillation to provide the titled compound (12 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06630469B2
출처 데이터셋uspto-grants-2003_10
ORD IDord-620bb07ad593457b905560cdc8f3a2c0
출처 메모uspto-grants-2003_10