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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Antimony trichloride | HCID 24814 | — |
| 반응물 | (Bis(2-methoxyethyl)amino)sulfur trifluoride | HCID 2734690 | — |
| 반응물 | 2-Methyl-5-[3-[4-(methylthio)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole | HCID 44481756 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-[3-[4-[(Fluoromethyl)thio]phenyl]-1-benzofuran-5-yl]-5-methyl-1,3,4-oxadiazole | HCID 68663962 | 30.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08492378B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-f89e108746f840ab95f83b7d38c22bb8 |
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| 출처 메모 | uspto-grants-2013_07 |
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