Method for preparing flavanone compound
A technology of compound and flavanone, which is applied in the field of preparation of flavanone compounds, can solve the problems of long reaction time and low yield, and achieve the effects of short reaction time, simple operation and easy promotion
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Embodiment 1
[0032] Example 1: Synthesis of flavanones based on bromo-n-butylpyridine
[0033] In a 50ml beaker, add 2'-hydroxychalcone 10mg, brominated n-butylpyridine (0.015g / ml) 0.05ml, NaOH (8mol / L) 0.05ml and H 2 O 10ml, stirred vigorously, controlled the temperature at 15°C, and reacted for 1.5h; the reacted mixture was extracted with benzene, then concentrated under reduced pressure; The peak area was measured at the peak 251nm, and the flavanone content was calculated, and the yield was 59.1%.
Embodiment 2
[0034] Example 2: Synthesis of flavanones based on bromo-n-butylpyridine
[0035] In a 50ml beaker, add 2'-hydroxychalcone 10mg, brominated n-butylpyridine (0.015g / ml) 0.10ml, NaOH (8mol / L) 0.10ml and H 2 O 10ml, stirred vigorously, the temperature was controlled at 20°C, and reacted for 2h; the reacted mixture was washed with CH 2 Cl 2 Extraction is carried out, and then concentrated under reduced pressure; after the concentrate is chromatographically separated, the peak area is measured at the characteristic peak of flavanones at 251 nm by high performance liquid chromatography, and the content of flavanones is calculated, and the yield is 89.4%.
Embodiment 3
[0036] Example 3: Synthesis of flavanones based on bromo-n-butylpyridine
[0037] In a 50ml beaker, add 2'-hydroxychalcone 10mg, brominated n-butylpyridine (0.015g / ml) 0.15ml, NaOH (8mol / L) 0.15ml and H 2 O 10ml, vigorously stirred, the temperature was controlled at 20°C, and reacted for 1.5h; the reacted mixture was extracted with ethyl acetate, and then concentrated under reduced pressure; The peak area was measured at 251 nm of the characteristic peak of ketone, and the content of flavanone was calculated, and the yield was 73.6%.
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