参与物
| 角色 | 名称 | HCID | 投料 |
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| 反应物 | 氯甲酸乙酯 | HCID 10928 | — |
| 反应物 | 6-氨基-2-甲基-3-硝基苯甲酸 | HCID 15283172 | — |
| 溶剂 | 吡啶 | HCID 1049 | — |
| 产物 | 6-Nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-one | HCID 15283173 | 79% |
反应步骤
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+).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US05428021 |
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| 来源数据集 | uspto-grants-1995_06 |
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| ORD ID | ord-7a5418f062a74240945f6ad1b316d8b0 |
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| 来源说明 | uspto-grants-1995_06 |
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