Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209560Generated: November 1, 2026

Pyrrole → 4,5-Dichloro-2-(3,4-dichlorophenyl)-1-(2-hydroxyethyl)-pyrrole-2-carbonitrile

https://huagongshe.com/reaction/2209560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrroleHCID 8027—
Reactant4,5-dichloro-2-(3,4-dichlorophenyl)-1H-pyrrole-3-carbonitrileHCID 183555—
ReactantEthanol, 1-bromo-HCID 14202443—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product4,5-Dichloro-2-(3,4-dichlorophenyl)-1-(2-hydroxyethyl)-pyrrole-2-carbonitrileHCID 19026377—

Reaction Steps

To a stirred mixture of 2.0 g (6.5 mmol) of 4,5-dichloro-2-(3,4-dichlorophenyl) -pyrrole-3-carbonitrile and 0.88 g (7.8 mmol) of potassium tert-butoxide heated at reflux in 50 mL of dioxane is added 0.98 g (7.8 mmol) of bromoethanol. The mixture is stirred at reflux for 12 hours, cooled, diluted with 50 mL of water, and extracted several times with chloroform. The combined chloroform extracts are dried over magnesium sulfate and concentrated in vacuo to leave a solid which, on warming and dissolving in ethyl acetate, deposits on cooling mostly starting pyrrole. Concentration of the mother liquor and recrystallization of the residual solid from 20% ethyl acetate in hexane gives 0.31 g of a white solid, mp 143°-145° C.; IR 5077A.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455263
Source datasetuspto-grants-1995_10
ORD IDord-4282a3bb49444536bd78ec3026ba2e76
Source noteuspto-grants-1995_10