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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 452699생성일: 2026년 10월 26일

Carbon Disulfide → 2-(2,3-Dihydro-1-benzofuran-5-yl)-5-[(3-fluoro-4-methoxybenzyl)thio]-1,3,4-oxadiazole

https://huagongshe.com/reaction/452699

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DisulfideHCID 6348—
반응물Potassium HydroxideHCID 14797—
반응물3-Fluoro-4-methoxybenzyl chlorideHCID 2060903—
반응물2,3-Dihydro-1-benzofuran-5-carbohydrazideHCID 18526469—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
생성물2-(2,3-Dihydro-1-benzofuran-5-yl)-5-[(3-fluoro-4-methoxybenzyl)thio]-1,3,4-oxadiazoleHCID 4459095467%

반응 단계

To a solution of 2,3-dihydro-1-benzofuran-5-carbohydrazide (356 mg, 2.00 mmol) and potassium hydroxide (85%, 198 mg, 3.00 mmol) in ethanol (15 mL) was added carbon disulfide (0.180 mL, 3.00 mmol), and the resulting mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure, a mixture of the obtained residue and N,N-dimethylformamide (10 mL) was tightly sealed in a vial, and the microwave was irradiated at 150° C. for 30 sec. After cooling to room temperature, 3-fluoro-4-methoxybenzyl chloride (698 mg, 4.00 mmol) was added, and the resulting mixture was stirred for 2 hr. The reaction mixture was diluted with ethyl acetate, washed twice with water and once with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was crystallized from hexane/ethyl acetate to give the title compound (478 mg, yield 67%) as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492378B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-7ecb29a39cb84233a9a132e3035b270c
출처 메모uspto-grants-2013_07