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Synthesis and Conformation Analysis of cis-1,2-Disubstituted Cyclododecanes

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【作者】 韩翔宇王明安李太公梁晓梅董燕红陈馥衡王道全

【Author】 HAN Xiang-Yu WANG Ming-An LI Tai-Gong LIANG Xiao-Mei DONG Yan-Hong CHEN Fu-Heng WANG Dao-Quan ② (Department of Applied Chemistry, China Agricultural University, Beijing 100094, China)

【机构】 Department of Applied Chemistry China Agricultural UniversityDepartment of Applied Chemistry China Agricultural UniversityBeijing 100094 China

【摘要】 cis-1,2-Disubstituted cyclododecanes 2 were synthesized by sodium borohydride reduction of 2-monosubstituted cyclododecanones and their structures were confirmed by 1H- NMR, 13C NMR and elemental analysis. The higher cis-selectivity of NaBH4 reduction of 2- monosubstituted cyclododecanones was rationalized by the mode of “corner position carbonyl participation”. Crystal data for 2c: Mr = 263.21, monoclinic, space group P21/c, a = 1.11140(7), b = 2.62590(17), c = 0.91360(6) nm, β = 106.1840(10)°, V = 2.5606(3) nm3, Dc = 1.366 g/cm3, Z = 8, F(000) = 1104, μ(MoKα) = 3.182 mm-1, S = 0.837, the final R = 0.0460 and wR = 0.1033. Crystal X-ray diffraction analysis for 2c showed that its ring skeleton adopts [3333] conformation, in which the OH group presents at the side-exo position and the other one at the corner carbon. The 1H NMR data of 2 showed that 1-corner-R-2-side-exo-OH [3333] and 1-corner-OH-2-side- exo-R [3333] conformations coexist in dynamic equilibrium in the solution, but only the former presents in the crystal.

【Abstract】 cis-1,2-Disubstituted cyclododecanes 2 were synthesized by sodium borohydride reduction of 2-monosubstituted cyclododecanones and their structures were confirmed by 1H- NMR, 13C NMR and elemental analysis. The higher cis-selectivity of NaBH4 reduction of 2- monosubstituted cyclododecanones was rationalized by the mode of “corner position carbonyl participation”. Crystal data for 2c: Mr = 263.21, monoclinic, space group P21/c, a = 1.11140(7), b = 2.62590(17), c = 0.91360(6) nm, β = 106.1840(10)°, V = 2.5606(3) nm3, Dc = 1.366 g/cm3, Z = 8, F(000) = 1104, μ(MoKα) = 3.182 mm-1, S = 0.837, the final R = 0.0460 and wR = 0.1033. Crystal X-ray diffraction analysis for 2c showed that its ring skeleton adopts [3333] conformation, in which the OH group presents at the side-exo position and the other one at the corner carbon. The 1H NMR data of 2 showed that 1-corner-R-2-side-exo-OH [3333] and 1-corner-OH-2-side- exo-R [3333] conformations coexist in dynamic equilibrium in the solution, but only the former presents in the crystal.

【基金】 Presented in part at the Third National Symposium of the Chinese Chemical Society on Organic Chemistry, Lanzhou, China, August, 2004 (for abstract, see Chin. J. Org. Chem., 2004, Suppl. 365);This project was supported by the National Natural Science Foundation of China (No. 20072053)
  • 【文献出处】 结构化学 ,Chinese Journal of Structural Chemistry , 编辑部邮箱 ,2007年06期
  • 【分类号】O623.11
  • 【被引频次】3
  • 【下载频次】47
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