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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 433059생성일: 2026년 10월 26일

Hydrochloric Acid → 6-Methoxy-3-nitropyridine-2-acetonitrile

https://huagongshe.com/reaction/433059

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-Methoxy-5-nitropyridineHCID 79525—
반응물2-(4-Chlorophenoxy)acetonitrileHCID 306444—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물6-Methoxy-3-nitropyridine-2-acetonitrileHCID 639510—

반응 조건

온도-12.5 °C

반응 단계

Under argon and in an anhydrous medium, 15 g (97.3 mmol) of 2-methoxy-5-nitropyridine and 17.9 g (107 mmol) of 4-chlorophenoxyacetonitrile are dissolved in 300 ml of anhydrous tetrahydrofuran; the solution is added by transfer to a solution of 24 g (214 mmol) of potassium tert-butylate in 220 ml of anhydrous tetrahydrofuran maintained at a temperature below −10° C. The reaction mixture is stirred for three hours at a temperature of from −10 to −15° C. An aqueous 5% hydrochloric acid solution (170 ml) is added dropwise to the reaction mixture, maintaining the temperature at —10° C. The mixture is extracted with ethyl acetate. After driving over magnesium sulphate and evaporation, the residue is purified by flash chromatography over silica gel (eluant:petroleum ether/ethyl acetate, 2:1). After washing with a petroleum ether/diethyl ether mixture (2:1), the title compound is obtained in the form of a brown product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06667304B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-b82b07e91cd34066aab64d64c177075c
출처 메모uspto-grants-2003_12