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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22406Erstellt: 24. Oktober 2026

Water → 3-Benzoylpyrrole

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1-Phenyl-2-propen-1-oneHCID 13028—
EduktSodium hydrideHCID 24758—
EduktTosylmethyl isocyanideHCID 161915—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-BenzoylpyrroleHCID 2773234—

Reaktionsschritte

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.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428053
Quelldatensatzuspto-grants-1995_06
ORD IDord-2ea31ed838e847d781bc94eb1500e415
Quellennotizuspto-grants-1995_06