関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Monoethyl malonate | HCID 70615 | — |
| 反応物 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 反応物 | (R)-4-bromo-alpha-methylbenzylamine | HCID 853000 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (R)N-[1-(4-Bromo-phenyl)-ethyl]-malonamic Acid Ethyl Ester | HCID 58762223 | 71.1% |
反応手順
To a magnetically stirred solution of (R)-(+)-1-(4-bromophenyl)ethylamine (0.51 g, 2.55 mmol) in anhydrous CH2Cl2 under argon and cooled to 0° C., were added ethyl hydrogen malonate (0.4 g, 3.06 mmol) EDC.HCl (0.58 g, 3.06 mmol) and HOBt (0.41 g, 3.06 mmol). The resulting solution was stirred at 25° C. overnight. CH2Cl2 was evaporate and residue partitioned between EtOAC and 1 N HCl. The organic layer was washed with H2O, brine and dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by flash column chromatography (40% EtOAc in hexanes) to provide the desired product (0.57 g, 71%) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07148226B2 |
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| 出典データセット | uspto-grants-2006_12 |
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| ORD ID | ord-b69fd6196b72414d81b4d2877f6e7555 |
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| 出典メモ | uspto-grants-2006_12 |
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