戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 71226作成日:2026年10月24日

Acrylonitrile → 3-(2-Oxo-1-phenylcyclohexyl)propanenitrile

https://huagongshe.com/ja/reaction/71226

反応式

関与物質

役割名称HCID仕込み量
反応物AcrylonitrileHCID 7855—
反応物2-PhenylcyclohexanoneHCID 95592—
溶媒1,4-DioxaneHCID 31275—
生成物3-(2-Oxo-1-phenylcyclohexyl)propanenitrileHCID 26338377.4%

反応手順

Triton B surfactant (500 μL) was added to a stirred solution of 2-phenylcyclohexanone (5 g, 28.7 mmol) in dioxane (40 mL). A solution of acrylonitrile (1.8 g, 33.9 mmol) in dioxane (5 mL) was added dropwise. A slight exotherm was observed. The solution was stirred at room temperature for 3 h and concentrated. The residue was diluted with EtOAc (50 mL) and washed with water (20 mL, 2×). The EtOAc extract was dried (MgSO4), filtered, and concentrated. The residual oil was chromatographed on a silica gel column. Elution with 2% EtOAc in heptane, followed by 5% EtOAc in heptane afforded 3-(2-oxo-1-phenylcyclohexyl)propanenitrile (5.05 g, 77% yield) as a colorless oil. HPLC: tR=2.73 min, YMC Combi S5 ODS 4.6×50 mm, 4 min gradient, Detection Wave length 220 nm, Starting solvent: 10% aq. MeOH—0.2% H3PO4; Final solvent: 90% aq. MeOH—0.2% H3PO4. LC/MS: m/e 228.26 (M+H)+, 250.14 (M+Na)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822510B2
出典データセットuspto-grants-2014_09
ORD IDord-3736b13c71b94907a71b3d1057a76994
出典メモuspto-grants-2014_09