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HRID 1364555作成日:2026年10月25日

4-(Methylsulfonyl)-3-(trifluoromethyl)benzonitrile → [4-Methanesulfonyl-3-(trifluoromethyl)phenyl]methanamine

https://huagongshe.com/reaction/1364555

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Methylsulfonyl)-3-(trifluoromethyl)benzonitrileHCID 45933716—
触媒NickelHCID 935—
溶媒AmmoniaHCID 222—
溶媒MethanolHCID 887—
生成物[4-Methanesulfonyl-3-(trifluoromethyl)phenyl]methanamineHCID 66632608—

反応手順

A mixture of 4-fluoro-3-trifluoromethylbenzonitrile (75 mg, 0.40 mmol), sodium sulfinate (44.5 mg, 0.44 mmol) in N,N-dimethylformamide (1.5 mL) was heated at 100° C. for 2 h. The reaction mixture was cooled to room temperature, quenched with water. The resulting white solid was collected via filtration, washed with cold water, dried in a vacuum oven to give 4-methanesulfonyl-3-trifluoromethyl-benzonitrile (90 mg, 90% yield). This benzonitrile was hydrogenated in 2N NH3 in methanol with 35 mg of Raney Ni under a hydrogen balloon for 2 h. The reaction mixture was filtered through a celite plug, washed with methanol, evaporated in vacuo to give the titled compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07888374B2
出典データセットuspto-grants-2011_02
ORD IDord-f6a0f34fb0a64f62a97a309ec3886341
出典メモuspto-grants-2011_02