51094-17-8

基本信息
中介四(4-羟基苯基)卟吩
5,10,15,20-四(4-羟苯基)卟啉
5,10,15,20-四(4-羟基苯基)卟啉
5,10,15,20-四(4-羟基苯)-21H,23H-卟啉
5,10,15,20-四(4-羟苯基)-21H,23H-卟吩
5,10,15,20-四(4-羟基苯基)-21H,23H-卟吩
5,10,15,20-四(4-羟苯基)-21H,23H-卟吩 1G
5,10,15,20-TETRAKIS(4-HYDROXYPHENYL)PORPHYRIN 5,10,15,20-四(4-羟苯基)卟啉
RARECHEM AS SA 0037
MESO-TETRA(P-HYDROXYPHENYL)PORPHINE
meso-Tetrakis(4-hydroxyphenyl)porphyrin
5,10,15,20-tetrakis(4-hydroxyphenyl)-21H
5,10,15,20-tetra(4-hydroxyphenyl)porphyrin
5,10,15,20-Tetrakis(4-hydroxyphenyl)porphyrin
5,10,15,20-TETRAKIS(4-HYDROXYPHENYL)-21H,23H-PORPHINE
5,10,15,20-TETRAKIS-(4-HYDROXYPHENYL)-21,23H-PORPHYRIN
5,10,15,20-Tetrakis(4-hydroxyphenyl)-21H,23H-porphyrin
物理化学性质
安全数据
制备方法

109-97-7

123-08-0

51094-17-8
将6.1g对羟基苯甲醛溶解于110mL丙酸中,加入6mL二甲基亚砜(DMSO),机械搅拌混合物并加热至128℃。将新蒸馏的3.5mL吡咯溶于10mL丙酸中,以每秒1滴的速度缓慢滴加至上述反应混合物中。随后将反应体系温度升至141℃,回流反应2小时。反应完成后,进行热过滤,用丙酸洗涤滤饼两次,得到蓝色固体5,10,15,20-四(4-羟基苯基)卟啉粗品。将10g干燥的粗产物置于100mL圆底烧瓶中,加入20mL无水乙醇,加热回流15分钟后,继续加热1.5小时。反应液冰浴冷却1.5小时,过滤,用乙醇洗涤两次,得到0.6172g 5,10,15,20-四(4-羟基苯基)卟啉,收率为7.27%。最后,通过硅胶柱层析(200目)纯化,使用丙酮作为洗脱液,得到纯化产物。
参考文献:
[1] Patent: CN105085536, 2018, B. Location in patent: Paragraph 0060; 0117-0122
[2] Journal of the American Chemical Society, 2013, vol. 135, # 49, p. 18513 - 18519
[3] Macromolecular Bioscience, 2013, vol. 13, # 6, p. 808 - 816
[4] Molecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals, 2001, vol. 364, p. 611 - 623
[5] Tetrahedron Letters, 2007, vol. 48, # 41, p. 7287 - 7290