HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355656Generated: October 28, 2026
2,3-Dichloroaniline → HCID 21829908, compound
https://huagongshe.com/reaction/355656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichloroaniline | HCID 11844 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 21829907 | HCID 21829907 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21829908 | HCID 21829908 | 21.9% |
Reaction Steps
Dimethylaminopyridine (50 mg) and dimethylaminopropylethylcarbodiimide hydrochloride (0.5 g) were added to a solution of 2-(1-ethyl-5-phenylimidazolidin-4-on-3-yl)isobutyric acid (0.6 g) prepared according to Example 8 in dichloromethane (15 mL) at 0° C. After stirring for 15 minutes at 0° C. to room temperature, 2,3-dichioroaniline (0.4 g) was added and the mixture was stirred overnight at room temperature. The reaction solution was poured into water whose pH was 2, and the mixture was extracted with chloroform. The organic layer was washed with water and dried over anhydrous sodium sulfate. After distilling off the solvent under reduced pressure, the resulting crude product was purified by thin-layer chromatography (silica gel, ethyl acetate/n-hexane=2/3) to give 0.2 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-74410d0b28b1468bb2961e81b34e9413 |
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| Source note | uspto-grants-1998_11 |
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