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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3080생성일: 2026년 10월 23일

Pyridine → (+/-)-(3R,4S)-4-Acetoxy-3-(2-chloropropionyloxy)tetrahydrofuran

https://huagongshe.com/ko/reaction/3080

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DichloromethaneHCID 6344—
반응물2-Chloropropionyl chlorideHCID 111019—
반응물(+/-)-(3R,4S)-3-hydroxy-4-methylcarbonyloxytetrahydrofuranHCID 22883851—
용매WaterHCID 962—
생성물(+/-)-(3R,4S)-4-Acetoxy-3-(2-chloropropionyloxy)tetrahydrofuranHCID 15789790—

반응 조건

온도23 °C

반응 단계

12.4 g of (±)-2-chloropropionyl chloride were added dropwise at 0°-5° C. to an ice-cooled mixture of 15.0 g of (±)-(3R,4S)-3-hydroxy-4-methylcarbonyloxytetrahydrofuran, 8.1 g of anhydrous pyridine and 200 ml of anhydrous dichloromethane. After addition was complete, the reaction mixture was stirred at 23° C. for a further 4 hours, after which it was poured onto 400 ml of water. The organic phase was then separated off, washed twice with 50 ml of water each time, dried over sodium sulfate and finally concentrated. The crude product was purified by distillation at a pressure of 10 mbar.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733850
출처 데이터셋uspto-grants-1998_03
ORD IDord-e6001659ddac4b01bf370c708fa8cdd0
출처 메모uspto-grants-1998_03