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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22406생성일: 2026년 10월 24일

Water → 3-Benzoylpyrrole

https://huagongshe.com/ko/reaction/22406

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Phenyl-2-propen-1-oneHCID 13028—
반응물Sodium hydrideHCID 24758—
반응물Tosylmethyl isocyanideHCID 161915—
용매Dimethyl SulfoxideHCID 679—
용매Diethyl EtherHCID 3283—
생성물3-BenzoylpyrroleHCID 2773234—

반응 단계

To a stirred suspension of sodium hydride (8.0 g) in 200 ml of dry ethyl ether was added dropwise a solution of phenylvinylketone (13.22 g) and tosylmethyl isocyanide (19.52) in 150 ml of dry methyl sulfoxide and 300 ml of dry ethyl ether at such a rate that the ether refluxed gently. After complete addition, the suspension was stirred at room temperature for 30 minutes and subsequently hydrolyzed by dropwise addition of 200 ml of water. The ether layer was separated and the aqueous layer extracted with ethyl acetate. The combined organic layers were washed with water, 0.1N sulfuric acid, and again with water. The organic phase was dried over magnesium sulfate, filtered and evaporated in vacuo. The residue was purified by flash column chromatography (silica gel, DCM/ethyl acetate, 5:1). The desired fractions were concentrated and the residual oil was crystallized from DCM/hexane, affording the product as crystals (7.11 g), m.p. 98°-99° C. (lit*m.p. 96°-97° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428053
출처 데이터셋uspto-grants-1995_06
ORD IDord-2ea31ed838e847d781bc94eb1500e415
출처 메모uspto-grants-1995_06