戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 573537作成日:2026年10月26日

Hexamethyldisilazane → {1-[3-(Methyloxy)phenyl]propylidene}propanedinitrile

https://huagongshe.com/reaction/573537

反応式

関与物質

役割名称HCID仕込み量
反応物HexamethyldisilazaneHCID 13838—
反応物3'-MethoxypropiophenoneHCID 584765—
反応物2-HydroxybutanedinitrileHCID 21253562—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物{1-[3-(Methyloxy)phenyl]propylidene}propanedinitrileHCID 8667184989.7%

反応条件

温度70 °C

反応手順

Hexamethyldisilazane (5.51 mL, 26.3 mmol) was added dropwise to acetic acid (11.30 mL, 197 mmol) at RT under nitrogen. The resulting solution was then added to a solution of 1-[3-(methyloxy)phenyl]-1-propanone (Description 1) (2.7 g, 16.44 mmol) and malonitrile (2.173 g, 32.9 mmol) in acetic acid (10 mL). The reaction mixture was stirred at 70° C. for 12 h. The reaction mixture was cooled to RT then diluted with water (30 mL), the aqueous layer was then extracted with DCM (3×50 mL) and the combined organic extracts were dried over a phase separating column and concentrated. Purification by chromatography on silica gel, eluting with a gradient of 0-20% ethyl acetate in cyclohexane, afforded the title compound (3.13 g). LCMS (A) m/z: 211 [M−1]−, Rt 1.40 min (basic).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029545B2
出典データセットuspto-grants-2015_05
ORD IDord-a7acaf093f1344639c977f05a053315f
出典メモuspto-grants-2015_05