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HRID 54869作成日:2026年10月23日

Dimethylformamide → (5R)-3-(4-methoxyphenyl)-5-phenyl-2-oxazolidinone

https://huagongshe.com/ja/reaction/54869

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1-Isocyanato-4-methoxybenzeneHCID 79443—
反応物(+)-Styrene oxideHCID 114705—
触媒Lithium ChlorideHCID 433294—
生成物(5R)-3-(4-methoxyphenyl)-5-phenyl-2-oxazolidinoneHCID 5389459353.8%

反応手順

3.50 g (29.1 mM) of (R)-(+)-styrene oxide, 0.035 g of lithium chloride and 14 ml of N,N-dimethylformamide (DMF) were placed in a 50 ml-three necked flask. Under refluxing and stirring in nitrogen atmosphere, a solution of 4.38 g (29.4 mM) of 4-methoxyphenyl isocyanate in 3.5 ml of DMF was added dropwise to the mixture in 40 minutes, followed by refluxing for 40 minutes under stirring. After the reaction, the reaction mixture was poured into ice water to precipitate a crystal. The crystal was recovered by filtration, washed with water and recrystallized from methanol. The resultant crystal was purified by silica gel column chromatography (eluent: toluene/ethyl acetate =100/1) and recrystallized from a toluene/methanol mixture solvent to obtain 4.22 g of (5R)-3-(4-methoxyphenyl)-5-phenyl-2-oxazolidinone (Yield: 53.8%). This compound showed the following phase transition series.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624600
出典データセットuspto-grants-1997_04
ORD IDord-533bfd7a4c5d4057b5b495e5fffe3c3b
出典メモuspto-grants-1997_04