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HRID 566262作成日:2026年10月26日

Bromoacetonitrile → beta-(R)-(2-fluorophenyl)-gamma,2-dioxo-4(R)-phenyl-3-oxazolidinebutyronitrile

https://huagongshe.com/reaction/566262

反応式

関与物質

役割名称HCID仕込み量
反応物BromoacetonitrileHCID 11534—
反応物Ammonium ChlorideHCID 25517—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
反応物3-[(2-fluorophenyl)-acetyl]-4(R)-phenyl-2-oxazolidinoneHCID 11150697—
溶媒TetrahydrofuranHCID 8028—
生成物beta-(R)-(2-fluorophenyl)-gamma,2-dioxo-4(R)-phenyl-3-oxazolidinebutyronitrileHCID 11089040—

反応条件

温度-30 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06174888B1
出典データセットuspto-grants-2001_01
ORD IDord-c2e93f265b024263bee5e9b284bba3b8
出典メモuspto-grants-2001_01