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HRID 234430생성일: 2026년 10월 25일

2-Methylfuran → N-[5-(2-methyl-5-furyl)thiophene-2-sulfonyl]pyrrole

https://huagongshe.com/reaction/234430

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylfuranHCID 10797—
반응물N-(5-bromothiophenesulfonyl)pyrroleHCID 23445587—
반응물HCID 178418306HCID 178418306—
촉매ZincchlorideHCID 3007855—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매TetrahydrofuranHCID 8028—
생성물N-[5-(2-methyl-5-furyl)thiophene-2-sulfonyl]pyrroleHCID 2299848119.3%

반응 조건

온도-10 °C

반응 단계

t-BuLi (1.7 m solution in hexane, 7.9 ml, 14.6 mmol) was added dropwise under constant stirring under a nitrogen atmosphere to a solution of 2-methylfuran (1.0 g, 12 mmol) in THF (20 ml) at -78° C. The solution was then warmed to -10° C. and stirring continued for 45 min. The solution was then added to a solution of zinc chloride (27 ml of a 0.5M solution in THF) at -30° C. and then warmed to room temperature where stirring continued for 1 hr. resulting in a pale yellow clear solution. The solution was then transferred via a steel canula under nitrogen to a solution of N-(5-bromothiophene-2-sulfonyl)pyrrole (Example 33A, 3.5 g, 12 mmol) and tetrakis(triphenylphosphine)-palladium (0) (693 mg, 0.6 mmol) in THF (15 ml) at -78° C. The solution was then warmed to room temperature and stirred for a period of 2 hours. Purification by column chromatography using 2% ethyl acetate gave 680 mg of N-[5-(2-methyl-5-furyl)thiophene-2-sulfonyl]pyrrole as a pale yellow powder (19% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05594021
출처 데이터셋uspto-grants-1997_01
ORD IDord-bcaac69dab8048f9bc83dbb0247428f4
출처 메모uspto-grants-1997_01