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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128755생성일: 2026년 10월 25일

Ethylene Oxide → 3-(3-Methylisoxazol-5-yl)propan-1-ol

https://huagongshe.com/reaction/128755

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene OxideHCID 6354—
반응물3,5-DimethylisoxazoleHCID 9312—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물3-(3-Methylisoxazol-5-yl)propan-1-olHCID 1001199245.9%

반응 조건

온도-75 °C

반응 단계

3,5-Dimethylisoxazole (220 g, 2.27 moles) in 2.2 L tetrahydrofuran under nitrogen was cooled with stirring to -75° C. and 908 mL of 2.5M n-butyllithium (2.27 moles) in hexanes were added over 1 hour keeping the temperature at or less than 65° C. The chilled solution was stirred for thirty minutes after addition was complete and was then treated at about -70° C. with a solution of 112 g (2.54 moles) of ethylene oxide in 390 ml tetrahydrofuran over a period of 1.5 hours, keeping the temperature at about -65° C. and stirred overnight. The mixture at 8° C. was quenched with continued cooling in an 8° C. bath by adding 1.2 L of 2.5M hydrochloric acid over a period of 20 minutes, during which time the temperature rose to 23° C., and was stirred for 10 minutes. The organic phase was separated, washed with 500 ml of water and concentrated to give 147 g of title compound as a brown oil. The combined aqueous phases (original+wash phase) were extracted with methyl tert-butyl ether (3×200 ml) and the combined organic extracts were concentrated to give an additional 125 g of title compound as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464848
출처 데이터셋uspto-grants-1995_11
ORD IDord-240b4490fb9d431dbfde66d54a9f7a8a
출처 메모uspto-grants-1995_11