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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 452782생성일: 2026년 10월 25일

Antimony trichloride → 2-[3-[4-[(Fluoromethyl)thio]phenyl]-1-benzofuran-5-yl]-5-methyl-1,3,4-oxadiazole

https://huagongshe.com/reaction/452782

반응식

참여 물질

역할이름HCID투입량
반응물Antimony trichlorideHCID 24814—
반응물(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
반응물2-Methyl-5-[3-[4-(methylthio)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazoleHCID 44481756—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물2-[3-[4-[(Fluoromethyl)thio]phenyl]-1-benzofuran-5-yl]-5-methyl-1,3,4-oxadiazoleHCID 6866396230.4%

반응 단계

To a solution of [bis(2-methoxyethyl)amino]sulfur trifluoride (1.38 mL, 7.50 mmol) in dichloromethane (10 mL) was added dropwise a solution of 2-methyl-5-[3-[4-(methylthio)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole (1.61 g, 5.00 mmol) in dichloromethane (15 mL) at room temperature. Antimony (III) chloride (0.0570 g, 0.250 mmol) was added to the solution, and the resulting mixture was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/tetrahydrofuran=1/1) and recrystallized from hexane/ethyl acetate to give the title compound (517 mg, yield 30%) as pale-yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492378B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-f89e108746f840ab95f83b7d38c22bb8
출처 메모uspto-grants-2013_07