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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1445758생성일: 2026년 10월 26일

Iodine → 2-(4-Bromo-phenyl)-4-(2-iodo-ethyl)-5-methyl-oxazole

https://huagongshe.com/reaction/1445758

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물PyridineHCID 1049—
반응물TriphenylphosphineHCID 11776—
반응물2-(2-(4-Bromophenyl)-5-methyloxazol-4-YL)ethanolHCID 10880530—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-(4-Bromo-phenyl)-4-(2-iodo-ethyl)-5-methyl-oxazoleHCID 58951394—

반응 조건

온도100 °C

반응 단계

Add iodine (1.90 g, 7.49 mmol) to a stirred mixture of 2-[2-(4-bromo-phenyl)-5-methyl-oxazol-4-yl]-ethanol (1.503 g, 5.33 mmol), triphenylphosphine (2.101 g, 8.01 mmol), and pyridine (1.4 mL, 17 mmol) in toluene (48 mL) and heat at 100° C. for 45 min. Cool to room temperature, add ethyl acetate and water, and separate the layers. Extract the aqueous layer twice with ethyl acetate, wash the organic layer with 0.1N HCl, dry over anhydrous magnesium sulfate, and concentrate under reduced pressure. Purify the residue by flash chromatography (SiO2, elute 0% to 10% EtOAc/hexanes) to-yield 1.804 g of the title compound as a colorless solid. 1H NMR (400 MHz, CDCl3) δ 7.89 (d, J=8.4 Hz, 2H), 7.60 (d, J=8.8 Hz, 2H), 3.49 (dd, J=7.2, 7.2 Hz, 2H), 3.11 (dd, J=7.2, 7.2 Hz, 2H), 2.39 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666871B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-ceb9f050bd8e44138dbb19c5551d1f16
출처 메모uspto-grants-2010_02