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HRID 1387706作成日:2026年10月27日

1,3-Dimethyl-2-imidazolidinone → (2S,3S)-2-allyl-3-hydroxy-gamma-butyrolactone

https://huagongshe.com/reaction/1387706

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Dimethyl-2-imidazolidinoneHCID 6661—
反応物Allyl chlorideHCID 7850—
反応物Ammonium ChlorideHCID 25517—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物3-Hydroxybutyrolactone, (3S)-HCID 7269389—
溶媒TetrahydrofuranHCID 8028—
生成物(2S,3S)-2-allyl-3-hydroxy-gamma-butyrolactoneHCID 2067547275%

反応条件

温度-45 °C

反応手順

Lithium hexamethyldisilazide (5.1 ml, 5.1 mmol) was loaded under argon gas in a reaction vessel. (S)-3-Hydroxy-γ-butyrolactone (0.250 g, 2.449 mmol) in THF (5 ml) was added thereto under cooling to −45° C. After stirring for 30 minutes at the same temperature, allyl chloride (0.24 ml, 2,94 mmol) and 1,3-dimethyl-2-imidazolidinone (0.7 ml) in THF (5 ml) was dropped thereto. After stirring for 30 minutes at the same temperature, an aqueous saturated ammonium chloride was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over magnesium sulfate, and condensed in vacuo. The residue was purified by silica gel chromatography to give (2S,3S)-2-allyl-3-hydroxy-γ-butyrolactone (0.261 g, yield 75%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06268515B1
出典データセットuspto-grants-2001_07
ORD IDord-bbbe6aecca904c5398a997f0604282ad
出典メモuspto-grants-2001_07