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HRID 53348作成日:2026年10月23日

Ammonium Chloride → (S,E)-3-(pent-2-enoyl)-4-phenyloxazolidin-2-one

https://huagongshe.com/ja/reaction/53348

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物2-Oxazolidinone, 4-phenyl-, (4S)-HCID 730424—
反応物(E)-pent-2-enoyl chlorideHCID 5706546—
反応物Sodium hexamethyidisilazaneHCID 45051731—
溶媒TetrahydrofuranHCID 8028—
生成物(S,E)-3-(pent-2-enoyl)-4-phenyloxazolidin-2-oneHCID 1109686328.7%

反応条件

温度-50 °C

反応手順

(S)-(+)-4-Phenyl-2-oxazolidinone (4.0 g, 24 mmol, Aldrich) was dissolved in dry THF (40 mL), and the solution was cooled to -50° C. and flushed with N2. Sodium hexamethyldisilazane (1.0M in THF, 25 mL, 25 mmol) was added slowly with stirring. The compound from step 7a (2.9 g, 24 mmol) was added slowly while maintaining the temperature at -50° C., and the mixture was stirred at this temperature for 1.5 hour. The mixture was allowed to warm to 0° C. and stirred for 1 hour. Saturated aqueous NH4Cl solution was added, the mixture was stirred for 10 minutes and the mixture was extracted with methylene chloride. The extract was dried over Na2SO4, filtered and the solvent was removed. The residue was chromatographed on silica gel, eluting with 2% methanol/methylene chloride, and the product was rechromatographed with 0.5% methanol/methylene chloride to give the title compound (1.69 g). MS m/ z 246 (M+H)+, 263 (M+NH4)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618949
出典データセットuspto-grants-1997_04
ORD IDord-54fbe7df9da8436eb7d74aeb74befc5f
出典メモuspto-grants-1997_04