تفاعل #2146693

معادلة التفاعل

2-(4′-benzoyloxyphenyl)-6-methoxyimidazo[1,2-a]pyridine

boron tribromide

methanol

→

2-(4′-hydroxyphenyl)-6-hydroxyimidazo[1,2-a]pyridine

المردود 89.5%

المذيبات

dichloromethane

ظروف التفاعل

المعالجة

1. 1
   أخرىto remove moisture
2. 2
   workup.DISSOLUTIONwas dissolved in 245 mL of chloroform
3. 3
   درجة الحرارةAfter the temperature of the resulting solution was raised to room temperature
4. 4
   أخرىAfter the completion of the reaction
5. 5
   درجة الحرارةthe reaction solution was cooled with ice
6. 6
   workup.STIRRINGfurther stirred at room temperature for 3 hours
7. 7
   تركيزThe reaction mixture was then concentrated under reduced pressure
8. 8
   أخرىto obtain slurry
9. 9
   أخرىprecipitates
10. 10
    ترشيحwere filtered
11. 11
    أخرىrecovered
12. 12
    أخرىThe precipitates recovered
13. 13
    غسيلwere washed with chloroform
14. 14
    أخرىdried under reduced pressure

الإجراء التجريبي

4.90 g (corresponding to 14.83 mmol) of 2-(4′-benzoyloxyphenyl)-6-methoxyimidazo[1,2-a]pyridine that was sufficiently dried to remove moisture was dissolved in 245 mL of chloroform and cooled down to −15° C. To this solution, a solution of 12.62 mL (corresponding to 133.48 mmol) of boron tribromide in 134 mL of dichloromethane was added dropwise. After the temperature of the resulting solution was raised to room temperature, the solution was stirred for 17 hours. After the completion of the reaction, the reaction solution was cooled with ice and supplemented with 668 mL of methanol, and further stirred at room temperature for 3 hours. The reaction mixture was then concentrated under reduced pressure. The resulting crude product was supplemented with 290 mL of chloroform and 29 mL of methanol to obtain slurry, and then precipitates were filtered and recovered. The precipitates recovered were washed with chloroform and then dried under reduced pressure, to obtain 3.00 g (corresponding to 13.28 mmol) of 2-(4′-hydroxyphenyl)-6-hydroxyimidazo[1,2-a]pyridine (FIG. 3, Step 6).

المصدر