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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1625725생성일: 2026년 10월 27일

Potassium Fluoride → HCID 66608418, 화합물

https://huagongshe.com/reaction/1625725

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참여 물질

역할이름HCID투입량
반응물Potassium FluorideHCID 522689—
반응물Tributyl-(4-ethylphenyl)stannaneHCID 60041267—
반응물4-(bromomethyl)-1-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)-1,2,3-triazoleHCID 66608307—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물HCID 66608418HCID 6660841817.1%

반응 조건

온도70 °C

반응 단계

A solution of 4-(bromomethyl)-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole 32 (500 mg) (See Federico G. H. et al., J. Med. Chem. (1979) 29, 496), tri-n-butyl(4-ethylphenyl)tin 33 (604 mg) and tetrakis(triphenylphosphine)palladium (0) (59 mg) in tetrahydrofuran (10 ml) was stirred under heating at 70° C. for 12 hours under argon atmosphere. The reaction mixture was cooled to room temperature, diluted with ethyl acetate, and then, an aqueous potassium fluoride solution was added thereto and the mixture was stirred at room temperature for one hour. Insoluble materials were filtered off, and the filtrate was washed with water, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=90:10-50:50) to give 4-(4-ethylphenylmethyl)-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,3-triazole 34 (90 mg) as a colorless solid. APCI-Mass m/Z 518 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08785403B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-4c60b556211e479ba1a287acf006ada8
출처 메모uspto-grants-2014_07