HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417481Generated: October 30, 2026
4-Chlorobenzoic Acid → Methyl 3-[((4-chlorobenzoyl)ethoxycarbonylmethylamino)methyl]-4-aminobenzoate
https://huagongshe.com/reaction/2417481
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzoic Acid | HCID 6318 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 3-[(ethoxycarbonylmethylamino)methyl]-4-nitrobenzoate | HCID 22632382 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3-[((4-chlorobenzoyl)ethoxycarbonylmethylamino)methyl]-4-aminobenzoate | HCID 69892547 | — |
Reaction Steps
2.2 g (6.14 mmol) of methyl 3-[(ethoxycarbonylmethylamino)-methyl]-4-nitrobenzoate was dissolved in 50 ml of dichloromethane. 4 mg (0.023 mmol) of 2-chloro-1,3-dimethylimidazonium chloride, 1.29 ml (9.2 mmol) of triethylamine and 1.16 g (7.3 mmol) of 4-chlorobenzoic acid were added to the obtained solution, and they were stirred overnight. After the treatment with dichloromethane as the extracting solvent by an ordinary method, the obtained crude product was dissolved in 20 ml of ethyl acetate. 200 mg of 10% palladium/carbon was added to the obtained solution and they were stirred in the presence of hydrogen at room temperature for 5 hours. The reaction mixture was filtered through Celite and the solvent was evaporated to obtain the crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825191B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-bf48037024d24fb3aa3fcfdd82d810bd |
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| Source note | uspto-grants-2004_11 |
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