31949-21-0

基本信息
α-溴-2'-甲氧基苯乙酮
2-溴-2'-甲氧基苯乙酮
Α-溴-2'-甲氧基苯乙酮
2-BROMO-2'-METHOXYACETOPHENONE
2'-METHOXYPHENACYL BROMIDE
2-METHOXYPHENACYL BROMIDE
A-BROMO-O-METHOXYACETOPHENONE
AKOS BBS-00003867
O-METHOXYPHENACYL BROMIDE
alpha-Bromo-o-methoxyacetophenone
Ethanone, 2-bromo-1-(2-methoxyphenyl)-
alpha-Bromo-2'-methoxyacetophenone
alpha-Bromo-2-methoxyacetophenone
bromomethyl 2-methoxyphenyl ketone
2-Methoxyphenacyl bromide 98%
2''-METHOXY-2-BROMOACETOPHENONE
2-BROMO-2''-METHOXYACETOPHENONE 98%
α-Bromo-2'-methoxyacetophenone
1-(2-Methoxyphenyl)-2-bromoethanone
1-(Bromoacetyl)-2-methoxybenzene
2'-Methoxy-α-bromoacetophenone
物理化學性質
安全數據
制備方法

579-74-8

31949-21-0
以2'-甲氧基苯乙酮為原料合成鄰甲氧基-2-溴苯乙酮的一般步驟如下:將溴化銅(II)(2.97 g,6.66 mmol)加入裝有回流冷凝器的雙頸圓底燒瓶中。向燒瓶中加入乙酸乙酯(10.0 mL),在氮氣保護下,將混合物于70℃攪拌5分鐘。緩慢加入1-(2-甲氧基苯基)乙酮(0.50 g,3.33 mmol)的氯仿(10.0 mL)溶液,隨后將反應混合物回流8小時。反應完成后,冷卻至室溫,通過硅藻土墊過濾,并用乙酸乙酯(20 mL)洗滌濾餅。將濾液減壓濃縮,得到的粗產物通過柱色譜法(洗脫劑比例為乙酸乙酯:己烷 = 1:4)進行純化,得到純品鄰甲氧基-2-溴苯乙酮(0.73 g,收率96%),為棕色液體。薄層色譜Rf值為0.43(展開劑比例為乙酸乙酯:己烷 = 1:4);1H NMR(300 MHz, CDCl3)δ: 7.81(1H, dd, J = 7.8, 1.8 Hz),7.52(1H, td, J = 7.8, 1.8 Hz),7.05-6.96(2H, m),4.61(2H, s),3.94(3H, s);13C NMR(75 MHz, CDCl3)δ: 192.3, 158.8, 134.9, 131.6, 124.9, 121.2, 111.7, 56.0, 38.0。
參考文獻:
[1] Bulletin of the Korean Chemical Society, 2017, vol. 38, # 12, p. 1481 - 1485
[2] Tetrahedron Letters, 2006, vol. 47, # 27, p. 4707 - 4710
[3] Tetrahedron Letters, 2009, vol. 50, # 6, p. 700 - 703
[4] Chemistry - A European Journal, 2011, vol. 17, # 28, p. 7953 - 7959
[5] Molecules, 2017, vol. 22, # 5,
報價日期 | 產品編號 | 產品名稱 | CAS號 | 包裝 | 價格 |
2025/05/22 | L07696 | 2-溴-2'-甲氧基苯乙酮, 98% 2-Bromo-2'-methoxyacetophenone, 98% | 31949-21-0 | 1g | 182元 |
2025/05/22 | L07696 | 2-溴-2'-甲氧基苯乙酮, 98% 2-Bromo-2'-methoxyacetophenone, 98% | 31949-21-0 | 5g | 910元 |
2025/05/22 | 14627 | 2-溴-2'-甲氧基苯乙酮 2-Bromo-2'-methoxyacetophenone, 98%, Thermo Scientific Chemicals | 31949-21-0 | 1g | 506元 |