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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 908098생성일: 2026년 10월 24일

Furamide → 4-(2,4-Dichloro-phenyl)-2-furan-2-yl-oxazole

https://huagongshe.com/ko/reaction/908098

반응식

참여 물질

역할이름HCID투입량
반응물FuramideHCID 69108—
반응물2-Bromo-1-(2,4-dichlorophenyl)ethan-1-oneHCID 75828—
반응물DiisopropylethylamineHCID 81531—
용매Hydrochloric AcidHCID 313—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물4-(2,4-Dichloro-phenyl)-2-furan-2-yl-oxazoleHCID 5812296955%

반응 조건

온도130 °C

반응 단계

To the solution of furan-2-carboxamide (56 mg, 0.5 mmol. 1 eq) and DIEA (0.13 mL, 0.75 mmo, 1.5 eq) in NMP (1 mL) was added 2-bromo-1-(2,4-dichlorophenyl)ethanone (0.6 mmol, 1.2 eq). Reaction mixture was heated at 130° C. for 15 h. The mixture was cooled down, diluted with 1 M HCl (30 mL) and extracted with EtOAc (40 mL). The organic layer was washed with 1 M HCl (30 mL), 5% solution of NaHCO3 (30 mL), brine (2×40 mL), dried over anhydrous Na2SO4, and concentrated in vacuo. The resulting residue was purified by HPLC purification to provide desired 4-(2,4-Dichloro-phenyl)-2-furan-2-yl-oxazole in a yield of 55% and HPLC 99.9% purity. LC-MS [M+H]-280.4 (C13H7Cl2NO2+H, requires 281.11). 1H NMR (DMSO-d6) δ 8.84 (s, 1H), 8.13 (d, 1H, J=8.5), 8.01 (s, 1H), 7.78 (s, 1H), 7.58 (d, 1H, J=8.5), 7.29 (d, 1H, J=3.5), 6.77 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08017555B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-33f47431745242a3b316dc4192a81ecd
출처 메모uspto-grants-2011_09