反应 #3198

ord-36369dc8420f49d692dad33fc33db94f

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他formed
  2. 2
    温度After refluxing this mixture for 1.5 hr
  3. 3
    温度it was cooled to room temperature
  4. 4
    过滤filtered
  5. 5
    其他to separate the solids
  6. 6
    workup.DISSOLUTIONThe solids were dissolved in rarer and the resulting solution
  7. 7
    其他to form a precipitate
  8. 8
    过滤The mixture was filtered
  9. 9
    洗涤the collected solids were washed with water and air
  10. 10
    其他dried

实验过程

A solution of methyl 2-amino-6-chlorobenzoate (3.00 g, 16.2 mM) and dimethyl acetylenedicarboxylate (2.64 g, 18.6 mM) in t-butanol (25 mL) was refluxed under a nitrogen atmosphere for 18 hr. The reaction mixture was cooled to room temperature and potassium t-butoxide (2.09 g, 18.6 mM) was added in one portion whereupon a precipitate formed. After refluxing this mixture for 1.5 hr, it was cooled to room temperature and filtered to separate the solids. The solids were dissolved in rarer and the resulting solution acidified with 1N H2SO4 to form a precipitate. The mixture was filtered and the collected solids were washed with water and air dried to give dimethyl 5-chloro-4-hydroxyquinoline-2,3-dicarboxylate (3.84 g, 80.2%) as a tan solid. An 0.25 g portion of this material was recrystallized from ethyl acetate to provide an analytical sample (0.152 g) of the title compound as an off-white solid, mp 174°-176° C.; MS(CI): 296 (M+H). Analysis for C13H10ClNO5.0.01 H2O: Calculated: C, 52.78; H, 3.41; N, 4.73 Found: C, 52.39; H, 3.38; N, 4.67

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05733910uspto-grants-1998_03