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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 724842생성일: 2026년 10월 26일

Acetic Acid → (2R,3S,4R,5R)-2-(hydroxymethyl)-5-(2,5,6-trichlorobenzimidazol-1-yl)oxolane-3,4-diol

https://huagongshe.com/reaction/724842

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물EthanolHCID 702—
반응물Sodium CarbonateHCID 10340—
반응물[(2R,3R,4R,5R)-3,4-diacetoxy-5-(2,5,6-trichlorobenzimidazol-1-yl)tetrahydrofuran-2-yl]methyl acetateHCID 466019—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물(2R,3S,4R,5R)-2-(hydroxymethyl)-5-(2,5,6-trichlorobenzimidazol-1-yl)oxolane-3,4-diolHCID 46509567.4%

반응 단계

To a solution of Na2CO3 (23.32 g, 220 mmol) in 440 mL of H2O were added successively 2.0 L of EtOH, 2.0 L of MeOH, and 105.5 g (220 mmol) of 42. The reaction mixture was stirred at room temperature for 2 hr. AcOH (26.44 mL 462 mmol) was added and stirring was continued at room temperature for 20 min. The reaction mixture was filtered. The solid product was triturated with H2O (800 mL 20 min), MeOH (500 mL 30 min), and then recrystallized from EtOH/MeOH (1 L/1 L) to give 52.4 g of 45 as white crystals {2 crops, the 2nd crop (2.8 g) was obtained by evaporation of the mother liquid and recrystallization of the residue two more times from EtOH/MeOH}. Recrystallization was accomplished by dissolving the crude product in a minimum amount of boiling EtOH, diluting it immediately with an equal amount of hot MeOH and allowing it to slowly cool. The filtrate was evaporated and the residue was triturated with H2O (500 mL, 20 min), MeOH (500 mL, 30 min), and then recrystallized twice from EtOH/MeOH to give an additional 15.34 g of 45 {2 crops, the 2nd crop (1.95 g) was obtained by evaporation of the mother liquid and recrystallization of the residue two more times from EtOH/MeOH}. The total of 45 was 67.74 g (87%). MP: 166°-168° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05705490
출처 데이터셋uspto-grants-1998_01
ORD IDord-883d1fc3ac9f40cca2a1d4f9e134453a
출처 메모uspto-grants-1998_01