戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2180327作成日:2026年10月27日

N-((1R,2R)-2-Amino-1,2-diphenylethyl)-4-methylbenzene-1-sulfonamide → 2-Chloro-1-[3-(dimethylamino)phenyl]ethan-1-ol

https://huagongshe.com/reaction/2180327

反応式

関与物質

役割名称HCID仕込み量
反応物N-((1R,2R)-2-Amino-1,2-diphenylethyl)-4-methylbenzene-1-sulfonamideHCID 2734565—
反応物2-Chloro-1-[3-(dimethylamino)phenyl]ethan-1-oneHCID 22491780—
反応物potassium t-butoxide IPAHCID 86592054—
溶媒IsopropanolHCID 3776—
生成物2-Chloro-1-[3-(dimethylamino)phenyl]ethan-1-olHCID 2249178295.5%

反応手順

A solution of di-μ-chlorodichlorobis(pentamethylcyclopentadienyl)dirhodium (III) (1.5 mg, 0.0025 mmol) and (1R,2R)-N-(p-toluenesulfonyl)-1,2-diphenylethylenediamine (3.7 mg, 0.01 mmol) in isopropyl alcohol (4.75 ml) was heated at 80° C. for 20 minutes while stirring. After cooling the solution to room temperature, a 0.1 M potassium tert-butoxide isopropyl alcohol solution (0.25 ml, 0.025 mmol) and 2-chloro-3′-(dimethylamino)acetophenone (98.8 mg, 0.5 mmol) as a reaction substrate were added thereto, followed by stirring at room temperature for 14 hours. After completion of the reaction, the solvent was removed by evaporation, and the residue was purified by silica gel column chromatography to give a desired compound, (+)-2-chloro-1-(3′-dimethylaminophenyl)ethanol (95.3 mg; yield: 95.3%; optical purity: 98.8% ee).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06888012B2
出典データセットuspto-grants-2005_05
ORD IDord-908a04923063430dae1cd9244c0a371f
出典メモuspto-grants-2005_05