戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2302176作成日:2026年10月26日

2-(4-Methoxyphenyl)-1,1-dimethylethylamine → (r)-n-[2-Hydroxy-3-(3-chloro-2-cyanophenoxy)propyl]-1,1-dimethyl-2-(4-methoxyphenyl)-ethylamine hydrochloride

https://huagongshe.com/reaction/2302176

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-Methoxyphenyl)-1,1-dimethylethylamineHCID 91892—
反応物(R)-2-chloro-6-(oxiran-2-ylmethoxy)benzonitrileHCID 44186486—
生成物(r)-n-[2-Hydroxy-3-(3-chloro-2-cyanophenoxy)propyl]-1,1-dimethyl-2-(4-methoxyphenyl)-ethylamine hydrochlorideHCID 986707980.2%

反応手順

Using the method of Example 6, supra, (R)-3-chloro-2-cyanophenyl glycidyl ether (0.7 g, 3.34 mmol) and 1,1-dimethyl-(4-methoxyphenyl)ethylamine (0.72 g, 4.0 mmol) were used to prepare 570 mg of the title compound as a white solid: 1H-NMR (CDCl3) 9.65 (1H, br s), 8.2 (1H, br s), 7.4 (1H, t), 7.15 (2H, d), 7.03 (1H, d), 6.95 (1H, d), 6.8 (2H, d), 4.8 (1H, m), 4.3 (2H, d), 3.75 (3H, s), 3.4 (2H, m), 3.13 (2H, dd), 1.44 (3H, s), 1.40 (3H, s); 13C-NMR 161.9, 159.4, 138.2, 135.1, 132.4, 126.8, 122.8, 114.4, 114.2, 111.6, 104.0, 71.8, 66.0, 61.9, 55.8, 45.4, 43.9, 23.5, 23.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06432656B1
出典データセットuspto-grants-2002_08
ORD IDord-b22ff6aad165445da3e5319fdbfd526e
出典メモuspto-grants-2002_08