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HRID 1877915作成日:2026年10月26日

Acetic Anhydride → 2,5-Dimethoxy-4-methylbenzonitrile

https://huagongshe.com/reaction/1877915

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物2,5-Dimethoxy-4-methylbenzaldehydeHCID 602019—
溶媒PyridineHCID 1049—
生成物2,5-Dimethoxy-4-methylbenzonitrileHCID 595738—

反応条件

温度105 °C

反応手順

By analogy to steps outlined in J. Med. Chem. 1976, 19(12), 1400-1404. 2,5-dimethoxy-4-methylbenzaldehyde (14.8 g, 82.2 mmol) is dissolved in pyridine (300 mL) and to it is added hydroxylamine hydrochloride (6.8 g, 98.6 mmol). The suspension is heated at 105° C. for 2 h. Acetic anhydride (15.5 mL, 164 mmol) is then added to the reaction and stirring is continued for another 2 h. The solution is evaporated to dryness and partitioned between EtOAc and saturated aqueous NaHCO3. The organic fraction is dried (Na2SO4) and evaporated to give a yellow solid which is taken up in hexanes and filtered to give 2,5-dimethoxy-4-methylbenzonitrile as a white solid. (cas # 51267-09-5) MS (ESI) m/z 178.2 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08314097B2
出典データセットuspto-grants-2012_11
ORD IDord-81ce424295a54c7d8d188675cf7c192a
出典メモuspto-grants-2012_11