3998-04-7
3998-04-7 結(jié)構(gòu)式
基本信息
9-Allyl-9H-carbazol
9H-Carbazole, 9-(2-propen-1-yl)-
物理化學(xué)性質(zhì)
制備方法
86-74-8
106-95-6
3998-04-7
以咔唑和3-溴-1-丙烯為原料合成9-烯丙基-9H-咔唑的一般步驟如下:首先,使用硫代苯甲酸S-[3-(9-咔唑基)丙基]酯(16)對1,2-聚丁二烯進行官能化反應(yīng),進而合成9-烯丙基咔唑(15)。具體操作如下:將咔唑(10.1g,0.057mol)和氫氧化鉀(88% wt顆粒,經(jīng)粉碎處理,7.1g,0.11mol)溶于100mL DMSO中,于50℃下攪拌30分鐘。隨后,緩慢滴加烯丙基溴(14.7g,0.118mol)。反應(yīng)15分鐘后,將混合物倒入含有100mL氯仿的500mL分液漏斗中,用200mL水洗滌5次。在60℃下減壓蒸發(fā)溶劑后,得到純度>99%的化合物15,為深棕色粘稠糖漿狀物,冷卻后固化為固體(11.9g,0.057mol,收率100%)。產(chǎn)物經(jīng)1H NMR (300MHz, CDCl3)分析顯示:δ=8.14-8.06 (m, 2H, 咔唑), 7.49-7.32 (m, 4H, 咔唑), 7.28-7.19 (m, 2H, 咔唑), 6.04-5.90 (m, 1H, CH=CH2), 5.19-5.10 (m, 1H, Z-HCH=CH), 5.07-4.97 (m, 1H, E-HCH=CH), 4.92-4.85 (m, 2H, NCH2)。13C NMR (300MHz, CDCl3)分析顯示:δ=140.34, 132.27, 125.67, 122.90, 120.33, 119.00, 116.74, 108.74, 45.21。
參考文獻:
[1] Patent: WO2009/52148, 2009, A1. Location in patent: Page/Page column 35
[2] Journal of Heterocyclic Chemistry, 2014, vol. 51, # 3, p. 683 - 689
[3] Synthetic Communications, 2010, vol. 40, # 15, p. 2291 - 2301
[4] Journal of the American Chemical Society, 2018, vol. 140, # 40, p. 12705 - 12709
[5] Russian Chemical Bulletin, 1993, vol. 42, # 8, p. 1372 - 1376