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HRID 353602作成日:2026年10月24日

Ammonium Chloride → 3-Chloromethyl-4-(4-fluoro-benzoyl)-benzonitrile

https://huagongshe.com/ja/reaction/353602

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物2-(Chloromethyl)-4-cyanobenzoyl chlorideHCID 11344910—
反応物Ethyl acetate hexaneHCID 21226206—
反応物HCID 178418676HCID 178418676—
溶媒TetrahydrofuranHCID 8028—
生成物3-Chloromethyl-4-(4-fluoro-benzoyl)-benzonitrileHCID 9943434—

反応手順

A solution of 4-fluoro phenylmagnesium bromide (3.76 g) in tetrahydrofuran (15 ml) was added to a cooled solution of 2-chloromethyl-4-cyano-benzoyl chloride (3.95 g) in tetrahydrofuran (10 ml) so that the temperature did not raise above 0° C. The mixture was warmed slowly to room temperature and stirred over night. Saturated ammonium chloride solution (60 ml) was added and stirring continued for 0.5 hours. The phases were separated and the aqueous phase was extracted with diethylether (30 ml). The combined organic phases were dried over sodium sulfate, filtered and dried in vacuo to give a brown solid. Flash chromatography (ethyl acetate/n-hexane=1/10) provided the product as colourless solid. Yield 2.95 g, 58%. 1H NMR (CDCl3, 400 MHz): 4.71 (2H, s), 7.16-7.21 (2H, m), 7.46 (1H, d, J=7.9 Hz), 7.71 (1H, dd, J=1.5, 7.9 Hz), 7.81-7.86 (2H, m), 7.89 (1H, d, J=1.5 Hz). 13C NMR (CDCl3, 100 MHz): 42.3, 115.0, 116.4, 116.6, 117.9, 129.6, 132.95, 132.98, 133.4, 133.5, 134.3, 138.7, 142.4, 165.5, 168.1, 194.5.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06753433B2
出典データセットuspto-grants-2004_06
ORD IDord-e922eef638ad42aaa2bcc784d588c265
出典メモuspto-grants-2004_06