HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1606659Erstellt: 26. Oktober 2026
Methylamine → 3-Metoxycarbonyl-5-nitrobenzoyl-glycine methylamide
https://huagongshe.com/reaction/1606659
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methylamine | HCID 6329 | — |
| Edukt | Chloroformic acid | HCID 164602 | — |
| Edukt | N-(3-Methoxycarbonyl-5-nitrobenzoyl)-glycine | HCID 21427264 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 3-Metoxycarbonyl-5-nitrobenzoyl-glycine methylamide | HCID 21427273 | — |
Reaktionsschritte
Process 2: 8.5 g. (0.03 mole) of N-(3-metoxycarbonyl-5-nitrobenzoyl-glycine (VIa) dissolved in 130 ml. of absolute tetrahydrofuran, is cooled to -15° C., after the addition of 4.2 ml. of triethylamine, and mixed under agitation with 3 ml. of the ethyl ester of chlorocarbonic acid. The reaction mixture is agitated for about 10 minutes at -10° to -5° C., and a solution of 2.8 ml. of methylamine in 20 ml. of absolute tetrahydrofuran, cooled to -15° C., is gradually added thereto dropwise under agitation. Then, the mixture is stirred for another 30 minutes at -15° C. and subsequently overnight at room temperature; the triethylamine hydrochloride is filtered off, the filtrate concentrated under vacuum, and the residue recrystallized from acetonitrile; yield 4.6 g. m.p. 173°-174° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US03953501 |
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| Quelldatensatz | uspto-grants-1976_04 |
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| ORD ID | ord-cff46c301bb1489bb5140c1444244d0c |
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| Quellennotiz | uspto-grants-1976_04 |
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