反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
2,4-Dinitro-1-(2-phenylchroman-6-yloxy)-benzene was prepared as described for 2-nitro-1-(2-phenylchroman-6-yloxy)-benzene in Example 29(a) except that 6-hydroxyflavane (0.226 g) was used in 5 ml of dry DMSO under nitrogen. Also KI (0.249 g) and KOH (0.112g) and 2,4-dinitrochlorobenzene (0.210 mg) were added in similar manner. Product was purified by column chromatography (CH2Cl2:n-heptane/75:25 as the eluant). 1H-NMR (400 MHz; d6-DMSO): δ 8.88 (d, 1H, J=2.8 Hz), 8.45 (dd, 1H, J=9.4 Hz, J=2.9 Hz), 7.48-7.30 (m, 5H), 7.14 (d, 1H, J=9.3 Hz), 7.10 (d, 1H, J=2.8 Hz), 7.05 (dd, 1H, J=8.8 Hz, J=2.9 Hz), 6.98 (d, 1H, J=8.7 Hz), 5.16 (dd, 1H, J=10.2 Hz, J=2.1 Hz), 3.08-2.93 (m, 1H), 2.83-2.71 (m, 1H), 2.25-2.13 (m, 1H), 2.08-1.94 (m, 1H).
WORKUP
后处理
- customProduct was purified by column chromatography (CH2Cl2