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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355652Generated: October 28, 2026

2,5-Dichloroaniline → HCID 18940316, compound

https://huagongshe.com/reaction/355652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DichloroanilineHCID 7262—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 21829916HCID 21829916—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
ProductHCID 18940316HCID 1894031622.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

Triphenylphosphine (1.3 g) was added to a suspension of 2-[4-methyl-2-oxo-3-(thiophen-3-yl)-3-pyrrolin-1-yl]isobutyric acid (1 g) in carbon tetrachloride (9 mL) and dichloromethane (9 mL), and the mixture was heated at reflux for 30 minutes at 70° C. After ice-cooling the reaction solution, 2,5-dichloroaniline (0.61 g) and then triethylamine (0.38 g) were added, and the mixture was stirred for 24 hours at room temperature. After the reaction was completed, distilling off the solvent, water was added and the resulting mixture was extracted with ethyl acetate. The extract was washed with diluted hydrochloric acid and a saturated sodium hydrogencarbonate aqueous solution, and dried over anhydrous sodium sulfate. After distilling off ethyl acetate, the resulting crude product was purified by preparative thin-layer chromatography (developing solvent: chloroform/ethyl acetate=20/1) to give 0.35 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834401
Source datasetuspto-grants-1998_11
ORD IDord-7df87e5300f8424586ffc8a405361b9a
Source noteuspto-grants-1998_11