反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
4-Bromoaniline (56.0 g., 0.33 Mol.), 2,5-hexanedione (37.6 g., 0.33 Mol), and acetic acid (5 ml) were placed into Toluene (500 ml) and heated under reflux for 8 hours employing a dean stark trap to remove the water from the reaction. The reaction was cooled to room temperature and concentrated under reduced vacuum. The resulting oil was taken into ethyl acetate, washed one time each with 2N hydrochloric acid, 2N NaOH, and H2O, dried over Na2SO4, and concentrated under reduced vacuum to yield a brown solid. Material was purified by silica gel flash chromatography eluting with hexane. Concentration of the appropriate fractions yielded 55.0 gm. of a light yellow solid. (68%) NMR was consistent with the proposed title structure. Field Desorption Mass Spectrum: M+ 249 m.p. 71°-73° C.
WORKUP
后处理
- temperatureheated
- temperatureunder reflux for 8 hours
- customto remove the water
- customfrom the reaction
- concentrationconcentrated under reduced vacuum
- washwashed one time each with 2N hydrochloric acid, 2N NaOH, and H2O
- dry with materialdried over Na2SO4
- concentrationconcentrated under reduced vacuum
- customto yield a brown solid
- customMaterial was purified by silica gel flash chromatography
- washeluting with hexane
- customConcentration of the appropriate fractions yielded 55.0 gm
- custom71°-73° C.