HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355652Generated: October 28, 2026
2,5-Dichloroaniline → HCID 18940316, compound
https://huagongshe.com/reaction/355652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,5-Dichloroaniline | HCID 7262 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 21829916 | HCID 21829916 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18940316 | HCID 18940316 | 22.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834401 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-7df87e5300f8424586ffc8a405361b9a |
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| Source note | uspto-grants-1998_11 |
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