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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901289Generated: October 30, 2026

Water → 3-Benzoylpyrrole

https://huagongshe.com/reaction/1901289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Phenyl-2-propen-1-oneHCID 13028—
ReactantSodium hydrideHCID 24758—
ReactantTosylmethyl isocyanideHCID 161915—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
Product3-BenzoylpyrroleHCID 2773234—

Reaction Steps

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. 6°-97° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576446
Source datasetuspto-grants-1996_11
ORD IDord-b9a409e131d14d9aa2fe991f0be90354
Source noteuspto-grants-1996_11