HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22182Erstellt: 23. Oktober 2026
Ethyl chloroformate → 6-Nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-one
https://huagongshe.com/de/reaction/22182
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | 6-Amino-2-methyl-3-nitrobenzoic acid | HCID 15283172 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 6-Nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-one | HCID 15283173 | 79% |
Reaktionsschritte
A solution of 4.0 g (20.4 mmoles) of 5-nitro-6-methyl-2-aminobenzoic acid in 50 mL of dry pyridine was cooled in an ice-water bath under inert atmosphere. Ethyl chloroformate (Aldrich), 10 mL (105 mmoles), was added dropwise over a 15 minute period. A mild exotherm was observed and a solid separated from solution immediately upon addition. The suspension was stirred at room temperature under inert atmosphere overnight. Approximately half the pyridine was removed in vacuo, and the residual mixture poured over ice. The precipitated solid was collected and air-dried. 4.0 g (79% yield) 6-nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-one was obtained. NMR (DMSO-d6): 1.37(t,3H,J=7.2 Hz), 2.71(s,3H), 4.50(q,2H,J=7.2 Hz), 7.40(d,1H, J=9.0 Hz), 8.19(d,1H,J=9.0 Hz). IR(nujol): 1765 cm-1 (lactone carbonyl). MS(m/z): 250(M+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05428021 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-7a5418f062a74240945f6ad1b316d8b0 |
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| Quellennotiz | uspto-grants-1995_06 |
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