HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19616Erstellt: 23. Oktober 2026
P-Phenylenediamine → [4-(4-Amino-phenylcarbamoyl)-benzyl]-carbamic acid tert-butyl ester
https://huagongshe.com/de/reaction/19616
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | P-Phenylenediamine | HCID 7814 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | 4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acid | HCID 853605 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | [4-(4-Amino-phenylcarbamoyl)-benzyl]-carbamic acid tert-butyl ester | HCID 67319189 | 55% |
Reaktionsschritte
To a solution of 4-(tert-butoxycarbonylamino-methyl)-benzoic acid (1.005 g) and N-hydroxy-benzotriazole (HOBt)(0.642 g) in DMF (30 ml) are added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC)(2.76 g) and triethylamine (2.005 ml). The mixture is stirred for 1 h at ambient temperature. This solution is added at 0° C. slowly to a solution of 1,4-diaminobenzene (0.43 g) and triethylamine (0.45 ml) in DMF (5 ml). After completion of the chemical reaction the mixture is evaporated at high vacuum and the residue is partitioned between ethyl acetate and an aqueous saturated sodium bicarbonate solution. The organic phase is dried over sodium sulfate and the crude product is purified by silica gel flash chromatography. A colorless solid (0.735 g) is obtained in 55% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745446B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-8d3603ac7c024e62b278797a849ef08e |
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| Quellennotiz | uspto-grants-2010_06 |
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