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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4408생성일: 2026년 10월 24일

Acetic Acid → 4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzonitrile

https://huagongshe.com/ko/reaction/4408

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물4-FluorobenzonitrileHCID 14517—
반응물Sodium hydrideHCID 24758—
반응물2-(5-Methyl-2-phenyl-4-oxazolyl)ethanolHCID 725585—
용매TetrahydrofuranHCID 8028—
생성물4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzonitrileHCID 1371397077.9%

반응 단계

2-(5-Methyl-2-phenyl-4-oxazolyl)ethanol (6.0 g) and 4-fluorobenzonitrile (5.4 g) were dissolved in tetrahydrofurane (70 ml ), and 60% sodium hydride in oil (1.4 g) was added to the solution under ice-cooling with vigorous stirring. The reaction mixture was stirred at room temperature for 18 hours and poured into ice-cold water (0.5 l). The aqueous mixture was neutralized with acetic acid, and the crystals which separated out were collected by filtration to give 4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzonitrile (7.0 g, 77.5%). Recrystallization from ether-hexane afforded colorless prisms, m.p. 119°-120° C. Elemental analysis for C19H16N2O2 ; Calcd: C, 74.98; H, 5.30; N, 9.20. Found: C, 74.90; H, 5.01; N, 9.28.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04725610
출처 데이터셋uspto-grants-1988_02
ORD IDord-ef7d7d2ba1b7436d9bffae2309e59136
출처 메모uspto-grants-1988_02