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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1046315생성일: 2026년 10월 25일

2-(4-Iodophenyl)oxazole → 2-[4-[(4-Methoxyphenyl)methyl]phenyl]oxazole

https://huagongshe.com/reaction/1046315

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Iodophenyl)oxazoleHCID 9860258—
반응물HCID 178490612HCID 178490612—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물2-[4-[(4-Methoxyphenyl)methyl]phenyl]oxazoleHCID 6848894981.5%

반응 단계

A Schlenk Flask was charged with tetrakis(triphenylphosphine)palladium(0) (0.42 g, 0.37 mmol), nitrogen, THF (20 ML), 2-(4-iodophenyl)oxazole (1 g, 3.7 mmol), and 4-methoxybenzyl zinc chloride (0.5 M in THF, 9.6 mL, 4.8 mmol). After 3 hours, the filtrate was concentrated. The resulting solid was treated with a mixture of ethyl acetate and a dilute aqueous ammonium chloride solution. The mixture was filtered and the organic layer was dried and concentrated. Purification on silica gel using a gradient of dichloromethane in hexane gave 0.8 g of 2-[4-[(4-methoxyphenyl)methyl]phenyl]oxazole, 1H NMR (400 MHz, CDCl3) δ 7.97 (d, 2H), 7.68 (s, 1H), 7.27 (d, 2H), 7.22 (s, 1H), 7.13 (d, 2H), 6.82 (d, 2H), 3.96 (s, 2H), 3.78 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569303B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-e5316016db224c899d4a8c7f7c1ebc90
출처 메모uspto-grants-2013_10