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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 327843Erstellt: 25. Oktober 2026

Water → 3-Benzoylpyrrole

https://huagongshe.com/reaction/327843

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
PatentnummerUS05274116
Quelldatensatzuspto-grants-1993_12
ORD IDord-6167e100e1f24ccbad6b3eec33a8c4a9
Quellennotizuspto-grants-1993_12