HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 359660Erstellt: 25. Oktober 2026
Hydrochloric Acid → N-(4-Carboxybenzyl)-(2-naphthoxy)acetamide
https://huagongshe.com/reaction/359660
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Chlorotrimethylsilane | HCID 6397 | — |
| Edukt | 2-Naphthoxyacetic acid | HCID 8422 | — |
| Edukt | 4-(Aminomethyl)Benzoic Acid | HCID 65526 | — |
| Edukt | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | N-(4-Carboxybenzyl)-(2-naphthoxy)acetamide | HCID 13922246 | — |
Reaktionsschritte
(2-Naphthoxy)acetic acid (8.5 g) is suspended in 160 mL methylene chloride and treated with 1,1'-carbonyldiimidazole (6.8 g) which is added in small portions. After stirring for 3 hrs at room temperature under a nitrogen atmosphere, the mixture is added dropwise to a previously prepared solution of alpha-amino-p-toluic acid (1.4 g), chlorotrimethylsilane (10 mL), and triethylamine (11 mL) in 250 mL methylene chloride at 0° C. The final mixture is stirred at room temperature under a nitrogen atmosphere overnight. The mixture is combined with 200 mL 1 N HCl and shaken, after which the resultant precipitate is collected by suction filtration. The precipitate is recrystallized from methanol/2N HCl, m.p. 188°-189° C. as N-(4-carboxybenzyl)-(2-naphthoxy)acetamide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05002703 |
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| Quelldatensatz | uspto-grants-1991_03 |
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| ORD ID | ord-0aa585abb3e4471a82cf99f8e131bd05 |
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| Quellennotiz | uspto-grants-1991_03 |
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