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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282343Generated: November 1, 2026

Iodoethane → HCID 18424230, compound

https://huagongshe.com/reaction/1282343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 18424368HCID 18424368—
SolventWaterHCID 962—
ProductHCID 18424230HCID 18424230—

Reaction Steps

A mixture of 24.4 g. (0.1 mole) 5-(p-chlorobenzyl)-pyrrole-2-acetonitrile, 41.7 g. (0.3 mole) of potassium carbonate and 16.1 g. (0.105 mole) of ethyl iodide in 300 ml. of methylethylketone is refluxed overnight. The reaction mixture is then poured into water and extracted with chloroform. The organic solutions are combined, dried over anhydrous magnesium sulfate, and the solvent evaporated in vacuo. The residue is crystallized from 2-propanol to give about 13 g. of crude solid. The solid is sublimed overnight at 140° C. and 0.025 mm. Hg. The sublimate is successively recrystallized from 2-propanol, benzene and hexane to give 5-(p-chlorobenzoyl)-1-ethylpyrrole-2-acetonitrile as a white solid, m.p. 145-147° C. Analysis: Calcd. for C15H13ClN2O: N, 10.2%. Found: N, 10.54%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455703B2
Source datasetuspto-grants-2002_09
ORD IDord-65c6bb5a1b8641fd9ed6135081c3a8b1
Source noteuspto-grants-2002_09