関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bromoacetonitrile | HCID 11534 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| 反応物 | 3-[(2-fluorophenyl)-acetyl]-4(R)-phenyl-2-oxazolidinone | HCID 11150697 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | beta-(R)-(2-fluorophenyl)-gamma,2-dioxo-4(R)-phenyl-3-oxazolidinebutyronitrile | HCID 11089040 | — |
反応手順
To a solution of 3-[(2-fluorophenyl)-acetyl]-4(R)-phenyl-2-oxazolidinone (435 g, 1.45 mol) in THF (6000 mL), is added sodium hexamethyldisilazide [(TMS)2 NNa, 1M in THF, 1480 ml, 1.48 mol] dropwise at −78° C. The resulting mixture is then warmed to −30° C. and stirred for 2.5 hours. After this time the reaction mixture is recooled to −78° C. and a solution of BrCH2CN (175 g, 1.46 mmol) in THF (200 mL) is added. The reaction mixture is then warmed to −40° C. and stirred for 2 hours. Subsequently the resulting solution is treated with saturated NH4Cl (1×3000 ml) and extracted with EtOAc (1×3000 mL). The organic layer is separated, washed with H2O (1×1500 mL), saturated NaCl solution (2×1500 mL), dried over MgSO4 and concentrated in vacuo, to provide 3-[(R)-β-cyano-α-(2-fluorophenyl)-propionyl]-4-(R)-phenyl-2-oxazolidinone, m.p. 179-181° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06174888B1 |
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| 出典データセット | uspto-grants-2001_01 |
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| ORD ID | ord-c2e93f265b024263bee5e9b284bba3b8 |
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| 出典メモ | uspto-grants-2001_01 |
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