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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 514630생성일: 2026년 10월 24일

Potassium Carbonate → HCID 89472347, 화합물

https://huagongshe.com/ko/reaction/514630

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,2,2-CryptandHCID 72801—
반응물Potassium FluorideHCID 522689—
반응물HCID 89472108HCID 89472108—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물HCID 89472347HCID 89472347—

반응 조건

온도80 °C

반응 단계

3.6 mg (7.6 μmol equivalents) of 2,2-dimethyl-5-[(4-methoxymethoxymethyl-2-nitro-1H-imidazol-1-yl)methyl]-5-(p-toluenesulfonyloxymethyl)-1,3-dioxane was dissolved in 1 mL of acetonitrile, 17 mg (34.5 μmol equivalents) of Kryptofix 222 (trade name, Merck), 5.8 mg (100 μmol equivalents) of potassium fluoride, and 1.8 mg (23 μmol equivalents) of potassium carbonate were added thereto, and the mixture was refluxed while heating for 3 hours. After completion of the reaction, water was added, and the mixture was extracted three times with chloroform. The combined chloroform layers were dried with anhydrous sodium sulfate and then concentrated under vacuum. The obtained crude product was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (v/v)=1/1). 1 mL of 1 mol/L hydrochloric acid was added dropwise to a fraction thus obtained, and the mixture was heated to 80° C. in an oil bath and then stirred for 50 minutes. After completion of the reaction, the mixture was concentrated under vacuum to give a trace amount of 1-(2,2-dihydroxymethyl-3-fluoropropyl)-4-hydroxymethyl-2-nitroimidazole.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09107964B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-32b6acceff8d494bbe86c5a677f48a98
출처 메모uspto-grants-2015_08