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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
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-sulfonamide | HCID 2734565 | — |
| 反応物 | 2-Chloro-1-[3-(dimethylamino)phenyl]ethan-1-one | HCID 22491780 | — |
| 反応物 | potassium t-butoxide IPA | HCID 86592054 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 2-Chloro-1-[3-(dimethylamino)phenyl]ethan-1-ol | HCID 22491782 | 95.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06888012B2 |
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| 出典データセット | uspto-grants-2005_05 |
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| ORD ID | ord-908a04923063430dae1cd9244c0a371f |
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| 出典メモ | uspto-grants-2005_05 |
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