HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374999Erstellt: 26. Oktober 2026
Dicyclohexylcarbodiimide → N-[2-(4-fluorobenzoyl)benzoyl]-N-methylglycine ethyl ester
https://huagongshe.com/reaction/374999
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | 2-(4-Fluorobenzoyl)benzoic acid | HCID 82099 | — |
| Edukt | Ethyl N-methylaminoacetate hydrochloride | HCID 171173 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | N-[2-(4-fluorobenzoyl)benzoyl]-N-methylglycine ethyl ester | HCID 21463059 | — |
Reaktionsschritte
A mixture of 2-(4-fluorobenzoyl)benzoic acid (3.00 g), 1-hydroxybenzotriazole (2.07 g), 1,3-dicyclohexylcarbodiimide (3.00 g) and anhydrous THF (50 ml) was stirred at room temperature for 1 hour. To this mixture were added N-methylglycine ethyl ester hydrochloride (2.84 g) and triethylamine (2.58 ml), followed by stirring at room temperature for 16 hours and with heating and refluxing for 4 hours. After the solvent was distilled off, ethyl acetate was added to the residue, and the insoluble crystals were separated by filtration. The filtrate was washed successively with water, aqueous sodium hydrogen carbonate, water, dilute hydrochloric acid and water and then dried, after which the solvent was distilled off, to yield N-[2-(4-fluorobenzoyl)benzoyl]-N-methylglycine ethyl ester as a colorless oily substance (4.2 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05482967 |
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| Quelldatensatz | uspto-grants-1996_01 |
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| ORD ID | ord-0ae52ed9dc254deaa9ffde3f0b954e69 |
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| Quellennotiz | uspto-grants-1996_01 |
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