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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1387706생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1387706

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Dimethyl-2-imidazolidinoneHCID 6661—
반응물Allyl chlorideHCID 7850—
반응물Ammonium ChlorideHCID 25517—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물3-Hydroxybutyrolactone, (3S)-HCID 7269389—
용매TetrahydrofuranHCID 8028—
생성물(2S,3S)-2-allyl-3-hydroxy-gamma-butyrolactoneHCID 2067547275%

반응 조건

온도-45 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06268515B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-bbbe6aecca904c5398a997f0604282ad
출처 메모uspto-grants-2001_07