2,2',7,7'-四溴-9,9'-螺双芴是化学合成、医药中间体,亦是合成光电材料的重要中间体。
化学合成; 医药; 光电材料
路线1:
- 步骤: 将80mg(0.5mmol)无水FeCl₃加入到3.16g(10.0mmol)9,9'-螺二芴的30ml二氯甲烷溶液中;在10分钟内滴加2.1ml(41mmol)溴溶于5ml二氯甲烷的溶液;将溶液回流6小时;冷却后产物沉淀,抽滤并用少量冷二氯甲烷洗涤,干燥得到目标产物。
- 条件: With FeCl₃; bromine In dichloromethane; 回流6小时
- 收率: 95%
- 参考文献: [1] Journal of the American Chemical Society, 1990, vol. 112, #14, p. 5662-5663; [2] Journal of Organic Chemistry, 1996, vol. 61, #20, p. 6906-6921; [3] Inorganic Chemistry, 2018, vol. 57, #11, p. 6210-6213; [4] Journal of Materials Chemistry A, 2016, vol. 4, #22, p. 8750-8754; [5] Chemistry - An Asian Journal, 2017, vol. 12, #2, p. 181-189; [6] Journal of Organic Chemistry, 2002, vol. 67, #14, p. 4924-4936; [7] Synthetic Communications, 2008, vol. 38, #12, p. 1888-1895; [8] Journal of Organic Chemistry, 2012, vol. 77, #4, p. 1663-1674; [9] Patent: US2003/111107, 2003, A1; [10] Patent: US5026894, 1991, A; [11] Patent: EP1053578, 2002, B1; [12] Journal of the American Chemical Society, 2008, vol. 130, #20, p. 6334-6335; [13] Journal of Materials Chemistry C, 2013, vol. 1, #11, p. 2183-2192; [14] Patent: CN106946750, 2017, A; [15] New Journal of Chemistry, 2018, vol. 42, #4, p. 2526-2536
路线2:
- 步骤: 将化合物2(10.6mmol,5g)溶解在150ml氯仿中,冷却至0℃,缓慢滴加溴(21.19mmol,3.39g),搅拌3小时;反应后注入50ml 2M氢氧化钾中和;用蒸馏水洗涤三次;分离有机层并真空蒸馏,用氯仿和乙醇混合溶液重结晶得到目标产物。
- 条件: With bromine In chloroform at 0℃; 3 h
- 收率: 85%
- 参考文献: [1] Patent: EP1777227, 2007, A1