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HRID 560551作成日:2026年10月26日

Cyanogen Bromide → HCID 178508456、化合物

https://huagongshe.com/reaction/560551

反応式

関与物質

役割名称HCID仕込み量
反応物Cyanogen BromideHCID 10476—
反応物Sodium HydroxideHCID 14798—
反応物N-BenzylethylenediamineHCID 77801—
溶媒EthanolHCID 702—
生成物HCID 178508456HCID 17850845696%

反応手順

To a solution of N-benzylethane-1,2-diamine (1.00 g, 6.65 mmol) in absolute ethanol (25 mL) was added cyanogen bromide (0.92 g, 8.65 mmol). The reaction mixture was stirred at ambient temperature for 1 hour, then cooled in an ice water bath. The pH of the solution was adjusted to ˜10 by the addition of 1 M sodium hydroxide solution dropwise. The solvent was concentrated in vacuo. The residue was diluted with ethyl acetate (100 mL), washed with water (200 mL) and brine (100 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and the concentrated in vacuo. The residue was recrystallized in ethyl acetate and hexane to yield the title compound as a colorless solid in 96% yield (1.12 g): mp 165-167° C. (ethyl acetate/hexanes); 1H NMR (300 MHz, DMSO-d6) δ 7.39-7.24 (m, 6H), 4.47 (s, 2H), 3.49-3.33 (m, 4H); 13C NMR (75 MHz, DMSO-d6) δ 159.4, 136.0, 129.1, 128.2, 128.1, 48.1, 47.4, 41.3; MS (ES+) m/z 176.3 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063084B2
出典データセットuspto-grants-2011_11
ORD IDord-4e673c1aeb2f403cab3e95cab44409aa
出典メモuspto-grants-2011_11