HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3565Erstellt: 23. Oktober 2026
Potassium Carbonate → methyl [N-(2-cyanophenyl)amino]acetate
https://huagongshe.com/de/reaction/3565
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Methyl bromoacetate | HCID 60984 | — |
| Edukt | 2-Aminobenzonitrile | HCID 72913 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | methyl [N-(2-cyanophenyl)amino]acetate | HCID 18917503 | 80,4% |
Reaktionsschritte
A mixture of 2.2 g of 2-cyanoaniline, 2.0 g of methyl bromoacetate and 1.3 g of potassium carbonate in 12 ml of dry N,N-dimethylformamide is heated at 150°-155° C. for 40 minutes. The cooled mixture is poured into ice-water and the mixture filtered to give 2 g of methyl [N-(2-cyanophenyl)amino]acetate as a yellow solid, m.p. 70°-78° C. The preceding compound (2.0 g) is added to a solution of 0.5 g of sodium methoxide in 50 ml of methanol. The mixture is shaken under an atmosphere of hydrogen with the catalyst Raney-Ni for 19 hours. The mixture is filtered through diatomaceous earth and the filtrate evaporated. Water is added to the residue and the mixture filtered to give 2,3,4,5-tetrahydro-1H-1,4-benzodiazepin-3-one as a yellow solid, m.p. 167°-170° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05733905 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-45712a7cc2764af2bb80289af78d8cd0 |
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| Quellennotiz | uspto-grants-1998_03 |
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