参与物
| 角色 | 名称 | HCID | 投料 |
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| 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 57346568 | 95.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US08084614B2 |
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| 来源数据集 | uspto-grants-2011_12 |
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| ORD ID | ord-2f1da52840a449cb8d6cbfcb5e7d9ad6 |
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| 来源说明 | uspto-grants-2011_12 |
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