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HRID 44133作成日:2026年10月24日

Trimethylsilyl cyanide → 1-Dimethylamino-4-(N',N'-dimethyl-hydrazino)-piperidine-4-carbonitrile

https://huagongshe.com/ja/reaction/44133

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethylsilyl cyanideHCID 82115—
反応物[4-(Dimethyl-hydrazono)-piperidin-1-yl]-dimethyl-amineHCID 67227495—
溶媒WaterHCID 962—
生成物1-Dimethylamino-4-(N',N'-dimethyl-hydrazino)-piperidine-4-carbonitrileHCID 6722836181.4%

反応手順

2.25 g [4-(Dimethyl-hydrazono)-piperidin-1-yl]-dimethyl-amine (from Step 1) is dissolved in 25 ml water, cooled in an ice bath, and 3.64 g trimethylsilyl cyanide is added at such a rate, that the internal temperature does not exceed 10° C. Then the mixture is stirred at ambient temperature for 18 hours, extracted with ethyl acetate, the organic layer washed with brine, dried over sodium sulfate, and the solvent evaporated, to give 2.1 g 1-Dimethylamino-4-(N′,N′-dimethyl-hydrazino)-piperidine-4-carbonitrile. 1H-NMR (CDCl3): 2.74 ppm (m, 2H), 2.50 ppm (m, 2H), 2.40 ppm (s, 6H), 2.35 ppm (s, broad, 1H), 2.24 ppm (s, 6H), 1.95 ppm (m, 2H), 1.60 ppm (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541343B2
出典データセットuspto-grants-2013_09
ORD IDord-5e9d866dabef4d8192a6503e58e2576a
出典メモuspto-grants-2013_09