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HRID 661663生成日期:2026年10月24日

甲酸 → 2-氯-3-氟苯甲酰胺

https://huagongshe.com/zh-CN/reaction/661663

反应方程式

参与物

角色名称HCID投料
反应物甲酸HCID 284—
反应物乙酐HCID 7918—
反应物2-氯-3-氟苯胺HCID 88884—
产物2-氯-3-氟苯甲酰胺HCID 5734656895.1%

反应条件

温度60 °C

反应步骤

A solution of acetic anhydride (10 mL, 106 mmol) and formic acid (30 mL, 795 mmol) was stirred at room temperature for 10 mins. 2-Chloro-3-fluoroaniline (2.9 g, 20 mmol) was added and the reaction mixture was stirred at 60° C. for 1.5 h. After cooling to room temperature, the solvents were removed in vacuo and the residue was redissolved in DCM (100 mL) and was washed with sat aq. NaHCO3 until the aqueous phase had a measured pH of 8. The organic layer was further washed with water (2×100 mL), separated and dried over MgSO4. Filtration and concentration in vacuo gave N-(2-chloro-3-fluoro-phenyl)-formamide (3.3 g, 95%) as a colorless solid which did not require further purification. MS (M+H)+: 173.9, tR=2.04 min (method 1).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08084614B2
来源数据集uspto-grants-2011_12
ORD IDord-2f1da52840a449cb8d6cbfcb5e7d9ad6
来源说明uspto-grants-2011_12