2369-13-3
952664-69-6
在0℃下,向3-氟-4-硝基苯胺(6.5g,42.2mmol)的乙酸(80mL)和氯仿(25mL)混合溶液中緩慢滴加溴(2.15mL,42.2mmol)。反應混合物在室溫下攪拌2小時后,倒入冰水中。在冰浴冷卻下,用10%氫氧化鈉水溶液調節(jié)混合物pH至8.0-9.0,隨后用乙酸乙酯(50mL ×3)萃取。合并有機相,依次用水(80mL ×2)和飽和食鹽水(100mL)洗滌,無水硫酸鈉干燥,減壓濃縮,得到2-溴-5-氟-4-硝基苯胺(9g,收率90%)。產(chǎn)物經(jīng)1H-NMR(400MHz,DMSO-d6)表征:δ8.26(d,J=8.0Hz,1H),7.07(brs,2H),6.62(d,J=9.6Hz,1H)。
參考文獻:
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[2] Patent: US2011/98311, 2011, A1
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