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N-Trimethylsilyl-N-methylacetamide → N-(2-hydroxy-1-phenylethyl)-benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-Trimethylsilyl-N-methylacetamide | HCID 81953 | — |
| 反応物 | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| 反応物 | (R)-beta-aminophenethyl alcohol | HCID 2724025 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(2-hydroxy-1-phenylethyl)-benzamide | HCID 14150746 | — |
反応手順
A slurry of (R)-2-amino-2-phenylethanol (1.0 g, 7.4 mmol) in 50 mL dichloromethane was allowed to stir with N-methyl-N-(trimethylsilyl)acetamide (3.4 mL, 21.1 mmol) until a homogenous solution occured. The solution was cooled to 0° C. to 5° C. and a solution of 2,2'-dithiobis[benzoyl chloride] (1.0 g, 2.9 mmol) in 20 mL dichloromethane was added. The solution was stirred for 2 hours and 1 mL of 50% aqueous acetic was added causing the crude product to precipitate from solution. This solid was collected by filtration, washed with 1N HCl, water, and recrystallized from dimethylformamide/water to afford 1.2 g of the title compound, mp 235°-236° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05734081 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-45e1e2f32fac4e2c92640fb69c3a608f |
| 出典メモ | uspto-grants-1998_03 |