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HRID 22182生成日期:2026年10月23日

氯甲酸乙酯 → 6-Nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-one

https://huagongshe.com/zh-CN/reaction/22182

反应方程式

参与物

角色名称HCID投料
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-oneHCID 1528317379%

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

DOI10.6084/m9.figshare.5104873.v1
专利号US05428021
来源数据集uspto-grants-1995_06
ORD IDord-7a5418f062a74240945f6ad1b316d8b0
来源说明uspto-grants-1995_06